Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
ACCESS TRAY/ASK-04001-SUH-S;
ACCESS TRAY/ASK-04001-VM1;
STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS;
STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS;
STIMUCATH SFTY KIT: 20G CTH, 18Gx8CM NDL/AB-20608-KS;
STIMUCATH KIT: 19G CATH, 17G x 9CM NDL/AB-05060-PK;
FLEXBLOCK ULTRASOUND KIT: 17Gx9CM NS NDL/ASK-19609-VCU;
CONTINUOUS NERVE BLOCK KIT/ASK-19600-CC2;
CONTINUOUS NERVE BLOCK KIT 19 GA X 60/ASK-19608-CC;
CONTINUOUS NERVE BLOCK KIT 19GA X 60CM/ASK-19608-KP;
CONTINUOUS NERVE BLOCK KIT 19GA X 60CM/ASK-19608-SHC;
FLEXBLOCK KIT:ECHO CATH, 17Gx8CM STM NDL/FB-19608-K;
FLEXBLOCK ULTRASOUND KIT: 17Gx8CM STM ND/FB-19608-KU;
FLEXBLOCK KIT:ECHO CATH, 17Gx9CM NS NDL/FB-19609-K;
FLEXBLOCK ULTRASOUND KIT: 17Gx9CM NS NDL/FB-19609-KU;
CONTINUOUS PERIPHERAL NERVE BLOCK KIT/ASK-19608-US1;
EPIDURAL CATHETERIZATION KIT/ASK-05001-SLR1;
EPIDURAL CATHETERIZATION KIT/MH-05001;
EPIDURAL CATHETERIZATION KIT/WJ-05401;
SPINAL ANES/EPIDURAL CATH 19GA X 90CM/ASK-05501-USC1;
EPIDURAL NEEDLE KIT/LG-03000;
EPIDURAL ANESTHESIA KIT/MTO-03000-VM;
EPIDURAL ANESTHESIA KIT/SM-03001;
Anesthesia conduction kit/FB-19611-K
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Anesthesia Conduction KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2364-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Biopsy Needle KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2365-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PACING PSI KIT: 6 FR/AI-06210-KS,
PACING PSI KIT: 5 FR 2-L/AI-07155-KS,
PACING PSI KIT: 5 FR 2L/ASK-07155-UPM
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Cardiac Catheterization KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2366-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB;
AGBA PICC G4 Stylet: 3L 6FR x 55CM TCG/DLX-45563-VPSC;
ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHD1;
ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHS1;
ARROW(R) VPS(R) ACCESS KIT/ASK-04001-DU13;
ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UNHS1
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Cardiovascular Procedure KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2367-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1;
RA CATH KIT: 20 GA X 1 1/2IN/NA-04220-S1A;
ARTERIAL LINE KIT/AK-04510-S;
ARTERIAL CATH KIT: 18 GA X 6IN (16 CM)/ASK-04018-HUMC;
ARTERIAL LINE KIT: 18 GA X 6 IN (16 CM)/ASK-04018-OH1;
RA CATH KIT: 20 GA X 1 3/4IN (4.45 CM)/ASK-04020-BID;
RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-MAR;
ARTERIAL LINE KIT: 20 GA X 5 IN/ASK-04020-PM4;
RA CATH KIT: 20 GA X 1 1/2IN (3.81 CM)/ASK-04120-HF3;
RA CATH SET: 20 GA X 2 1/2 IN (6.35 CM)/ASK-04120-UR;
ARTERIAL CATH KIT: 20 GA X 3 1/16 IN/ASK-04125-MGH;
ARTERIAL CATH KIT: 20 GA X 5 IN/ASK-04500-HFH4;
ARTERIAL LINE KIT: 20GA X 5IN/ASK-04510-BID2;
ARTERIAL LINE KIT: 20GA X 5IN (12 CM)/ASK-04510-EHP1;
ARTERIAL LINE KIT/ASK-04510-FEM1;
ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-HFH;
ARTERIAL CATH KIT: 20 GA X 5 IN/ASK-04510-HFH4;
ARTERIAL LINE KIT/ASK-04510-SE;
ARTERIAL LINE KIT: 20 GA X 5 IN (12CM)/ASK-04510-TGH2;
RA CATH KIT: 20 GA X 12 CM/NA-04550-1A;
RA CATH KIT: 20 GA X 12 CM/NA-04550-X1A;
RA CATH KIT: 18 GA X 1-3/4IN/AK-04018;
RA CATH KIT: 20 GA X 1-3/4IN/AK-04020;
RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-C;
RA CATH KIT: 20 GA X 1-1/2IN/AK-04120;
RA CATH KIT: 22 GA X 1-3/8IN/AK-04122;
RA CATH KIT: 20 GA X 1-1/2IN/AK-04220;
RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-AH;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-ATH;
RA CATH KIT: 20 GA X 1 3/4IN (4.45CM)/ASK-04020-AU2;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-BHS;
ARTERIAL CATHETERIZATION KIT/ASK-04020-BIDB2;
RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-CCD1;
ARTERIAL CATHETERIZATION KIT/ASK-04020-CR;
ART LINE KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-EUH2;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-FAM1;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-FMC;
RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-KSF2;
RA CATH KIT: 20 GA X 1 3/4 IN (4.5 CM)/ASK-04020-LHC2;
RA CATH KIT: 20 GA X 1 3/4 IN (4.5 CM)/ASK-04020-LHC3;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-LM;
RA CATH KIT: 20 GA X 1 3/4IN/ASK-04020-MCH1;
RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MIH1;
RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-NWMX;
RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-PHP;
RA CATH KIT: 20 GA X 1-3/4 IN (4.45CM)/ASK-04020-RIHM;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-RMC1;
RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-RU;
RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-SE;
RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-SHM;
RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-SRMC1;
RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-UCL1;
RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-UMI;
RA CATH KIT: 20 GA X 1-3/4 IN (4.45CM)/ASK-04020-UN;
RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-UNC;
RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-UNC1;
RA CATH SET: 20 GA X 1-1/2IN (3.81CM)/ASK-04220-PSU;
RA CATH KIT: 20 GA X 1-1/2 IN (3.81 CM)/ASK-04220-UCL1;
RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-S1A;
CVC KIT: 20 GA X 5 IN (12CM)/ASK-04550-JMC1;
ARTERIAL ACCESS TRAY/ASK-04001-BW2;
ARTERIAL ACCESS TRAY WITH .025 IN SWG/ASK-04001-WUH1;
ARTERIAL LINE KIT/ASK-04510-HUM
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH;
PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU4;
PSI/CVC KIT: 9 FR/7 FR X 6IN (16CM)/ASK-09903-AMC1;
PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-CMC1;
PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU4;
PSI KIT: 9 FR X 4 1/8 IN (10CM)/ASK-09903-PCMH1;
PSI KIT: 8.5 FR X 10 CM/CDC-09803-1A;
PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-ECL3;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-11242-PHP2;
MULTI LUMEN/PSI KIT/ASK-11142-NSU;
MULTI-LUMEN/PSI KIT/AK-21242-X;
MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-DMC;
MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-GMC1;
MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-HF5;
MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-LMDT;
2L MAC KIT: 9 FR DISTAL X 4IN (10 CM)/ASK-21142-UCL1;
2-L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-UPMC2;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-SL1;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMH;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UN1;
MAC KIT: 2-L 9 FR DISTAL X 10 CM AGB/CDC-21142-XCN1A;
MAC KIT: 2-L 9 FR DISTAL X 10 CM AGB/CDC-21142-XN1A;
MAC KIT: 2-L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-XCN1A;
MAC KIT: 2-L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-XN1A;
2L MAC KIT: 9 FR DISTAL X 4 IN/ASK-21142-CO1;
2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-FH3;
2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-OHSU3;
MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-SG2;
MULTILUMEN/MAC KIT: 9 FR X 4 IN (10 CM)/ASK-21142-UOI1;
2 LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-WHC2;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-BID1;
AGB MAC KIT: 2L 9 FR DISTAL/ASK-21242-BSWH2;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-DU1;
MULTILUMEN/PSI KIT 9 FR X 11.5 CM/ASK-21242-PCMH1;
MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UCH2;
AGB MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UHC2;
PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-BSWH2;
PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-HHC;
PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-MCY1;
PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-UPM1;
PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29804-VCU;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-MCY1;
PSI KIT: 9 FR/ASK-29903-MHI;
PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-OHU4;
PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-UCH2;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UCL1;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UHC4;
PSI KIT: 9FR X 4IN (10 CM) ANTIMICROBIAL/ASK-29903-UPM1;
PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-29907-LGH;
PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-1A;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-1A;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-X1A;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-XCN1A;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-XN1A;
PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-AHH;
PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-XN1A;
PSI ACCESS TRAY/ASK-04001-MM2;
MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-GMC;
MULTI LUMEN/PSI KIT: 9 FR DISTAL X 4 1/2/ASK-21242-OSU3
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS
AGBA PICC/DELTA: 2L 5.5 FR X 50 CM/ASK-45052-NS
AGBA PICC/DELTA KIT: 1L 4.5 FR X 55 CM/ASK-45541-MHBV
PICC KIT: 2L 5.5 FR X 55 CM CG+ VPS/ASK-45552-RH
AGBA PICC NaviCurve: 2L 5.5FR x 55CM BP/DLX-45552-CURVB
AGBA PICC NaviCurve: 2L 5.5FR x 55CM TCG/DLX-45552-CURVC
AGBA PICC: 2L 5.5FR x 55CM w Biopatch/DLX-45552-HPKB
AGBA PICC NaviCurve: 3L 6FR x 55CM BP/DLX-45563-CURVB
PI PICC KIT: 4 FR X 50 CM/ASK-35041-NH
PI PICC KIT: 2-L 5 FR X 50 CM/ASK-35052-NH
PI PICC G4 Stylet: 1L 4FR x 55CM w CHG/DLX-35541-VPSC
PI PICC NaviCurve: 2L 5FR x 55CM w BP/DLX-35552-CURVB
PI PICC NaviCurve: 3L 6FR x 55CM w BP/DLX-35563-CURVB
PI PICC G4 Stylet: 3L 6FR x 55CM w BP/DLX-35563-VPSB
AGBA PI PICC KIT: 2L 5.5 FR X 55CM/CDC-45552-HPK1A
PI AGBA PICC KIT: 3-L 6 FR X 55 CM/CDC-45563-HPK1A
PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI1
PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-VFH1
PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI1
PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-VFH1
PI AGBA PICC KIT: 3L 6 FR X 55 CM W/VPS/ASK-45563-UWH1
AGBA PICC NaviCurve: 1L 4.5FR x 55CM BP/DLX-45541-CURVB
AGBA PICC NaviCurve: 1L 4.5FR x 55CM TCG/DLX-45541-CURVC
AGBA PICC G4 Stylet: 1L 4.5FR x 55CM TCG/DLX-45541-VPSC
AGBA PICC G4 Stylet: 2L 5.5FR x 55CM BP/DLX-45552-VPSB
AGBA PICC G4 Stylet: 2L 5.5FR x 55CM TCG/DLX-45552-VPSC
PI PICC:1L 4FR X 50CM PRELOAD VPS STYLET/CDC-35041-VPS
PICC KIT: 3 FR X 55 CM/CDC-05531-PK1A
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter Repair KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2370-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1;
EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501;
EPIDURAL CATHETERIZATION KIT/AK-05502;
EPIDURAL CATHETERIZATION KIT/AK-05502D;
EPIDURAL CATHETERIZATION KIT/AK-05503;
EPIDURAL CATHETERIZATION KIT/AK-05503-L;
SPINAL ANES/EPIDURAL CATH KIT/AK-05560;
SPINAL ANES/EPIDURAL CATH KIT/ASK-02520-SBMC1;
EPIDURAL CATHETERIZATION KIT/ASK-05400-BW1;
EPIDURAL CATHETERIZATION KIT/ASK-05400-GH;
SPINAL ANES/EPIDURAL CATH KIT/ASK-05401-LMC;
EPIDURAL CATHETERIZATION KIT/ASK-05401-NM;
SPINAL ANES/EPIDURAL CATH KIT/ASK-05500-BID1;
EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-JHH1;
EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-MCV1;
EPIDURAL CATHETER KIT: 19GA X 90CM ASK-05500-MVH;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-UMC;
19 GA X 35.5 IN EPIDURAL CATHETER KIT/ASK-05502-MLH;
SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-JMH1;
SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-MKD2;
SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-OM1;
EPIDURAL CATHETERIZATION KIT/ASK-17019-SM;
EPIDURAL CATHETERIZATION KIT/BP-05501;
EPIDURAL CATHETERIZATION KIT/CK-05401;
EPIDURAL CATHETERIZATION KIT/HS-05501;
EPIDURAL CATHETERIZATION KIT/MM-05501;
EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TK;
EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKD;
EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKL;
EPIDURAL CATHETERIZATION KIT/MSO-05401-JMH;
EPIDURAL CATHETERIZATION KIT/NM-05401;
EPIDURAL CATHETERIZATION KIT/SJ-05501;
EPIDURAL CATHETERIZATION KIT/SM-05401;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/TM-05401;
EPIDURAL CATHETERIZATION KIT/TM-05502;
SPINAL ANES/EPIDURAL CATH KIT/UI-05502;
SPINAL ANES/EPIDURAL CATH KIT: 19 GA/ASK-05400-SHM;
EPIDURAL CATH KIT: 19 GA/ASK-05400-UOM;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-MR;
EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-TM;
EPIDURAL CATHETERIZATION KIT/ASK-05501-BHL1;
EPIDURAL CATHETERIZATION KIT/ASK-05501-GH;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-SM;
EPIDURAL CATHETERIZATION KIT/ASK-05502-BSM;
EPIDURAL CATHETERIZATION KIT/ASK-05502-MGH1;
EPIDURAL CATHETERIZATION KIT/ASK-05503-BWB1;
EPIDURAL CATHETERIZATION KIT/ASK-05503-HMH;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-SPH;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-UPM1;
SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-UCI2;
EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-17019-UMP;
EPIDURAL CATHETERIZATION KIT/MH-05503-1;
EPIDURAL CATHETERIZATION KIT/ASK-05401-VB2;
Epidural Catheterization Kit: 19GA/ASK-05500-SC1;
Epidural Catheterization Kit: 19GA/ASK-05500-SC3;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-AFH1;
EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-BMC;
EPIDURAL CATHETERIZATION KIT/ASK-05502-NY;
EPIDURAL CATHETERIZATION KIT/ASK-17019-RMH
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Multi-Lumen Hemodialysis Catheterization KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2372-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F;
HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122;
HEMODIALYSIS KIT 2L: 14 FR X 15CM AGB/AK-22142-CDC;
HEMODIALYSIS KIT 2L: 14 FR X 20CM AGB/AK-25142-CDC;
HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UMD;
HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UNC;
HEMODIALYSIS KIT: 2L 14 FR X 20 CM/ASK-25142-UMD;
HEMODIALYSIS KIT 2L: 14 FR X 20 CM AGB/ASK-25142-UN1;
HEMODIALYSIS KIT: 2L 14 FR X 25 CM/ASK-26142-UMD;
HEMODIALYSIS KIT: 2LUMEN 12 FR X 13 CM/AU-23122-F;
HEMODIALYSIS KIT: 2LUMEN 12 FR X 20 CM/AU-25122-F;
HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-X1A;
HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-XU1A;
HEMODIALYSIS KIT: 2L 14 FR X 15 CM AGB/CDC-22142-X1A;
HEMODIALYSIS KIT: 2L 12 FR X 25 CM AGB/CDC-26122-X1A;
HEMODIALYSIS KIT 2L: 12 FR X 16CM AGB/AK-22122-CDC;
HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122-F;
HEMODIALYSIS KIT: 2-LUMEN 14 FR X 15 CM/AK-22142-F;
AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-CN1AU;
AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-CN1AC;
AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-CN1AU;
AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-CN1AU;
AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-CN1AC;
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, Hemodialysis, Non-ImplantedDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2373-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC;
AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC;
AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A;
AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XP1A;
AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPN1A;
AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-XN1A-U;
LBCVC AGB KIT: 3-L 12 FR X 16 CM/CDC-22123-XN1A
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, Hemodialysis, Triple Lumen, Non-ImplantedDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2374-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2;
PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PNHS2;
PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PNHS2
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: I.V. Start KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2375-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH;
CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F;
CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F;
3L CVC KIT: 7 FR X 16 CM/ASK-12703-PMAH;
3L PI CVC KIT: 7 FR X 16 CM/ASK-12703-PNM;
3L CVC KIT: 7 FR X 16 CM/ASK-12703-PUMH;
MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-15703-PRH;
MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/CDC-15703-P1A;
PI CVC KIT: 3-L 7 FR X 6IN (16 CM)/NA-12703-PCDC;
PI CVC KIT: 3-L 7 FR X 8IN (20 CM)/NA-15703-PCDC;
CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-25553;
2-L CVC KIT: 4 FR X 5 CM/CDC-22402-X1A;
2-L CVC KIT: 5 FR X 5 CM/CDC-22502-X1A;
2-L CVC KIT: 4 FR X 8 CM/CDC-25402-X1A;
2-L CVC KIT: 5 FR X 8 CM/CDC-25502-X1A;
3-L CVC KIT: 5.5 FR X 8 CM/CDC-25553-X1A;
3-L CVC KIT: 5.5 FR X 13 CM/CDC-26553-X1A;
CVC KIT 3L: 12 FR X 16 CM AGB/AK-22123-CDC;
CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-22123-F;
CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-22402;
CVC KIT: 2-LUMEN 5 FR X 5 CM/AK-22502;
CVC KIT: 16 GA X 8IN/AK-24301-SK;
CVC KIT: 2-LUMEN 4 FR X 13 CM/AK-24402;
CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-24703-ASK;
CVC KIT 3L: 12FR X 20 CM AGB/AK-25123-CDC;
CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-25123-F;
CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-25402;
CVC KIT: 2-LUMEN 5 FR X 8 CM/AK-25502;
CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-26553;
LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-1A;
LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-X1A;
CVC KIT: 16 GA X 20 CM/CDC-24301-1A;
PI CVC KIT: 2L 7 FR X 16 CM AGB/AK-22702-P1A;
PI CVC KIT: 2L 7 FR X 16 CM AGB/CDC-22702-XP1A;
CVC KIT: 3L 7 FR X 20 CM/ASK-45703-CPR;
MULTILUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-AKP1A;
MULTI-LUMEN PI CVC KIT: 3-L 7 FR X 6IN/ASK-42703-KH;
PI CVC KIT: 3L 7FR X 16CM AGB+/ASK-42703-MGH1;
MULTI LUMEN PI CVC KIT: 3L 7 FR X 6IN/ASK-42703-PCCH2;
PI CVC KIT: 3LUMEN 7 FR X 6IN (16 CM)/ASK-42703-PFS1;
PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNO2;
MULTI LUMEN PI CVC KIT: 3L 7 FR/ASK-42703-PSCH1;
MULTILUMEN PI CVC KIT: 2L 8 FR X 16 CM/ASK-42802-AKP1A;
CVC KIT: 2L 8 FR X 16CM/ASK-42802-LMDTG1;
PI CVC KIT: 2L 8 FR X 6 IN (16 CM) AGB+/ASK-42802-PUCI1;
PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PUMH;
PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-UMM;
PI CVC KIT: 4-L 8.5 FR X 6 IN/ASK-42854-AKP1A;
PI CVC KIT: 4L 8.5FR X 16CM AGB+/ASK-42854-MGH;
MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-AKP1A;
PI CVC KIT: 3L 7 FR X 20CM AGB+/ASK-45703-MGH;
MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PCCH2;
MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PECL1;
PI CVC KIT: 3 LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PFS1;
PI CVC KIT: 3L 7 FR X 8 IN (20 CM) AGB+/ASK-45703-PHM1;
PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PHU;
PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PMSG1;
MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PNCB;
MULTILUMEN CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PPCM;
PI CVC KIT: 3-LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PRH;
MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PSJ2;
PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PSVM;
MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PUHS;
PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PUKL;
PI CVC KIT: 3L 7FR X 20CM AGB+/ASK-45703-PUMF1;
PI CVC KIT: 3L 7 FR X 8 IN (20 CM)/ASK-45703-PUR1;
PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-RHR1;
MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-WA;
MULTI LUMEN PI CVC KIT: 2L 8 FR X 8 IN/ASK-45802-AKP1A;
PI CVC KIT: 4L 8.5 FR X 20 CM/ASK-45854-AKP1A;
PI CVC KIT: 4L 8.5FR X 20CM AGB+/ASK-45854-MGH;
PI CVC KIT: 4L 8.5 FR X 8IN/ASK-45854-PCCH2;
CVC KIT: 4L 8.5 FR X 20 CM AGB/ASK-45854-PNM;
MULTI LUMEN CVC KIT: 4L 8.5 FR X 8 IN/ASK-45854-PPCM;
PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PUCH2;
MULTILUMEN PI CVC KIT: 2L 7 FR X 20 CM/ASK-46702-PWBH1;
MULTILUMEN CVC KIT: 2L 8 FR X 16 CM/CDC-42802-P1A;
PI CVC KIT: 3-L 7 FR X 20 CM AGB/CDC-45703-PA1A;
CVC KIT: 2L 8 FR X 6IN (16 CM)/ASK-42802-ECL4;
PI CVC KIT: 3-L 7 FR X 16 CM AGB+/AK-42703-P1A;
PI CVC KIT: 2-L 8 FR X 16 CM AGB+/AK-42802-P1A;
PI CVC KIT: 4-L 8.5 FR X 16 CM AGB+/AK-42854-P1A;
PI CVC KIT: 3-L 7 FR X 20 CM AGB+/AK-45703-P1A;
PI CVC KIT: 2-L 8 FR X 20 CM AGB
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6
RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-X1ASP
ACCESS TRAY/ASK-04001-MS
RA CATH KIT: 20 GA X 8 CM/ASK-00820-UM1
VESSEL CATH KIT: 20GA X 5IN/AK-04550-S
CVC KIT: 1-LUMEN 5 FR X 20 CM/AK-04301-SP
CVC KIT: 16 GA X 6IN (16 CM)/AK-04306-SP
CVC KIT: 16GA X 6 IN/AK-04800-S
CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-12402
CVC KIT: 3-LUMEN 7 FR X 16 CM/AK-12703-CDC
CVC KIT: 2L 4 FR X 13 CM/AK-14402
CVC KIT: 2-LUMEN 5 FR X 13 CM/AK-14502
CVC KIT: 3-LUMEN 5.5 FR X 30 CM/AK-14553
CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-14703-SP
CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-15402
CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-15553
CVC KIT: 2-LUMEN 4 FR X 30 CM/AK-16402
CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-16553
CVC KIT: 5 FR X 20 CM/ASK-04301-HH2
CVC KIT 3L: 7 FR X 6 IN (16 CM)/ASK-12703-MGH3
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, PercutaneousDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2377-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC;
AGBA PICC: 2L 5.5 FR X 45 CM/ASK-44552-ABKB;
AGBA PICC/DELTA KIT: 5.5 FR X 55 CM/ASK-45552-MHBV;
AGBA PICC: 1L 4.5FR x 55CM w Biopatch/DLX-45541-HPKB;
PICC/DELTA KIT: 2L 5.5 FR X 50 CM/ASK-45052-MC;
AGBA PI PICC KIT: 1L 4.5FR 40CM/CDC-44041-HPK1A;
AGBA PI PICC KIT 2-LUMEN: 5.5 FR X 40CM/CDC-44052-HPK1A;
AGBA PICC/DELTA FG: 2-L 5.5 FR X 40 CM/CDC-44052-VPS2;
PI AGBA PICC KIT: 3-L 6 FR X 50 CM/CDC-45063-HPK1A;
AGBA PICC/DELTA KIT: 1-L 4.5 FR X 55 CM/CDC-45541-VPS2;
AGBA PICC/DELTA FG: 2-L 5.5 FR X 55 CM/CDC-45552-VPS2;
PICC/VPS 1L 4.5 FR/ASK-45541-CHS;
PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI2;
PICC KIT: 2L 5.5FR 55CM AGBA VPS/ASK-45552-CHS;
PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI2;
PICC KIT: 3L 6FR 55CM AGBA/ASK-45563-CHS;
PI JACC KIT: 3L 6 FR X 25 CM CG+/ASK-42563-LTAC;
PI JACC KIT: 1-L 4.5 FR X 25 CM CG+/CDC-42541-JX1A;
PI JACC KIT: 2-L 5.5 FR X 25 CM CG+/CDC-42552-JX1A;
PI JACC KIT: 3-L 6 FR X 25 CM CG+/CDC-42563-JX1A;
PI JACC KIT: 2-L 5.5 FR X 30 CM CG+/CDC-43052-JX1A;
PI JACC KIT: 3-LUMEN: 6 FR X 30 CM CG+/CDC-43063-JX1A;
PICC KIT: 2-L 4 FR X 55 CM/CDC-05542-PK1A
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2378-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC;
PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC;
AGBA PI JACC KIT: 1-L 4.5 FR X 15 CM/CDC-41541-JX1A;
AGBA PI JACC KIT: 2-L 5.5 FR X 15 CM/CDC-41552-JX1A;
AGBA PI JACC KIT: 3-L 6 FR X 15 CM/CDC-41563-JX1A;
AGBA PI JACC KIT: 1-L 4.5 FR X 20 CM/CDC-42041-JX1A;
AGBA PI JACC KIT: 2-L 5.5 FR X 20 CM/CDC-42052-JX1A;
AGBA PI JACC KIT: 3-L 6 FR X 20 CM/CDC-42063-JX1A
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, Ultrasound, IntravascularDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2379-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, PeritonealDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2380-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Catheter, SubclavianDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2381-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
DRAINAGE KIT/AK-01600,
DRAINAGE KIT/AK-01601,
DRAINAGE KIT/ASK-01601-MM,
THORACENTESIS KIT/AK-01000-T,
THORACENTESIS KIT/AK-01000,
THORACENTESIS KIT/ASK-01000-CHP,
DRAINAGE KIT/ASK-01000-NW,
THORACENTESIS KIT/ASK-01000-UPMS,
PNEUMOTHORAX KIT/AK-01500,
PNEUMOTHORAX KIT (NO HEIMLICH VALVE)/ASK-01500,
PNEUMOTHORAX KIT/ASK-01500-JCM
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Chest Drainage KitDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2382-2026
Open, ClassifiedPosted Jun 13, 2026·Initiated Apr 21, 2026
Description/REF:
PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU
Reason: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Root cause: Nonconforming Material/Component
Recalling firm: ARROW INTERNATIONAL, LLCType: Electrode, Pacemaker, TemporaryDistribution: US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR.Recall #Z-2383-2026