Open, ClassifiedPosted Apr 9, 2025·Initiated Mar 5, 2025
MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980R
Reason: Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Root cause: Under Investigation by firm
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: Electrosurgical, Cutting & Coagulation & AccessoriesDistribution: US Nationwide distributionRecall #Z-1549-2025
Open, ClassifiedPosted Apr 9, 2025·Initiated Mar 11, 2025
BD Pyxis MedBank CUBIE Replenishment Station
Product / Material ID
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 155141-01
BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P / 155140-01
BD PYXIS MEDBANK TWR MN CR-12HH-1FH / 155142-01
BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P / 155143-01
BD PYXIS MEDBANK TWR MN CR-14HH-P / 155144-01
BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM / 155145-01
BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P / 155156-01
BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P / 155157-01
BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P / 155151-01
BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P / 155152-01
BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P / 155153-01
BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P / 155154-01
BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P / 155155-01
BD PYXIS MEDBANK TWR MN CR-2HH-6FH / 155146-01
BD PYXIS MEDBANK TWR MN CR-2HH-6FM / 155147-01
BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P / 155148-01
BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P / 155149-01
BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P / 155150-01
BD PYXIS MEDBANK MINI CR-2HH-1FH-P / 169-114
BD PYXIS MEDBANK MINI CR-4HH-P / 169-115
BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P / 169-82
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 169-83
BD PYXIS MEDBANK TWR MN CR-12HH-1FH / 169-84
BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P / 169-85
BD PYXIS MEDBANK TWR MN CR-14HH-P / 169-86
BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM / 169-87
BD PYXIS MEDBANK TWR MN CR-2HH-6FH / 169-88
BD PYXIS MEDBANK TWR MN CR-2HH-6FM / 169-89
BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P / 169-90
BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P / 169-91
BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P / 169-92
BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P /169-93
BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P / 169-94
BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P / 169-95
BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P / 169-96
BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P / 169-97
BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P / 169-98
BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P / 169-99
BD PYXIS MEDBANK MINI CR-2HH-1FH-P / 138913-01
BD PYXIS MEDBANK MINI CR-4HH-P / 138911-01
BD PYXIS MEDBANK MN 200 CR-2HH-1FH-P / 139001-01
BD PYXIS MEDBANK MN 200 CR-2HH-1FM-P / 139002-01
BD PYXIS MEDBANK MN 200 CR-4HH-P / 139000-01
BD PYXIS MEDBANK MN 500 CR-2HH-1FM-2DD-P / 139020-01
BD PYXIS MEDBANK MN 500 CR-2HH-5FM-P / 139018-01
BD PYXIS MEDBANK MN 500 CR-4HH-1FH-3FM-P / 139019-01
BD PYXIS MEDBANK MN 500 CR-4HH-4FM-P / 139021-01
BD PYXIS MEDBANK MN 500 CR-6HH-3FM-P / 139022-01
BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P / 138973-01
BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P / 138975-01
BD PYXIS MEDBANK TWR MN CR-12HH-1FH / 139073-01
BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P / 138976-01
BD PYXIS MEDBANK TWR MN CR-14HH-P / 138977-01
BD PYXIS MEDBANK TWR MN CR-2HH-1FH-5FM / 138951-01
BD PYXIS MEDBANK TWR MN CR-2HH-6FH / 139072-01
BD PYXIS MEDBANK TWR MN CR-2HH-6FM / 139085-01
BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P / 138968-01
BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P / 138964-01
BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P / 138966-01
BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P /138967-01
BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P / 138969-01
BD PYXIS MEDBANK TWR MN CR-6HH-8HM-P / 138965-01
BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P / 138971-01
BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P / 138972-01
BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P / 138974-01
BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P / 138970-01
BD Pyxis QFill Replenishment Station / 138904-01
KIT BD PYXIS QFILL REPLENISHMENT STATION / 155197-01
MEDBANK UPOS211 AIO WIN10 QFILL 1.5 / 155215-05
OPT,MEDBANK,HD,WIN10,QFILL,CR / 131944-04
The BD Pyxis" MedBank" CUBIE" Replenishment Station is an Automated Dispensing Cabinet (ADC) that is intended to be used by a qualified and authorized user to replenish medications and supplies to a BD Pyxis" MedBank" cabinet.
Reason: Due to a software issue, when attempting to restock the automated dispensing cabinet, user have received the banner message "Stocking window has passed, or item has been removed from purchase order. Please contact Pharmacy for assistance". When this occurs, the medication cannot be restocked and can potentially lead to delays in accessing medication for patients.
Root cause: Device Design
Recalling firm: CareFusion 303, Inc.Type: Cabinet, Table And Tray, AnesthesiaDistribution: U.S.: AL,AZ, CA, CT, FL, GA, IA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, PA, TN, TX, UT, VA, WA, WI and WV.
O.U.S.: NoneRecall #Z-1550-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless Steel, Catalog Number MRUE200, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1534-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1535-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1536-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Instrument Check Block, Catalog Number MRUE203, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1537-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Box Base, Catalog Number MRUE204, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1538-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Glenoid Box Lid, Catalog Number MRUE205, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1539-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Depth Stop Pin, Catalog Number MRUE206; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1540-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1541-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 5, 2025
stryker HoloBlueprint Application, Catalog Number MRUE001; Total Shoulder Arthroplasty
Reason: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Root cause: Device Design
Recalling firm: Tornier S.A.S.Type: Orthopedic Stereotaxic InstrumentDistribution: US: TX, MN, AK, PA, MA, TN, ID, and France, Canada, and IrelandRecall #Z-1542-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 4, 2025
Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model 977119) and Intellis Pro (Model 977118) neurostimulators
Reason: There is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used.
Root cause: Under Investigation by firm
Recalling firm: Medtronic NeuromodulationType: Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefDistribution: Worldwide Distribution: US (Nationwide) and OUS (Global) to countries of: Austria, Belgium, Bulgaria, Canary Islands, Cyprus, Croatia, Czech Republic, Denmark, Finland,
France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Japan, Luxembourg, Malta, Netherlands, Northern Ireland, Norway, Poland, Portugal, Puerto Rico, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey, and United Kingdom.Recall #Z-1543-2025
Open, ClassifiedPosted Apr 8, 2025·Initiated Mar 20, 2025
GenetiSure Dx Labeling Kit, REF: K1201-64105, contains human reference DNA female aliquot, REF5190-7317. A required kit for the GenetiSure Dx Postnatal assay (K1201A).
Reason: DNA Labeling Kit for use in sample labeling to be hybridized to oligonucleotide microarrays has a component, Human Reference DNA Female aliquot, affected by a mosaic aberration that may result in Chromosome 12 baseline shift, which may lead to false positive/negative results, resulting in diagnosis delay, and may lead to delayed treatment of a treatable genetic disorder.
Root cause: Nonconforming Material/Component
Recalling firm: Agilent Technologies, Inc.Type: System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality DetectionDistribution: US distribution to the state of: MA and OUS (International) distribution to countries of: Spain, Italy, Japan, Colombia, PolandRecall #Z-1544-2025 Open, ClassifiedPosted Apr 7, 2025·Initiated Feb 26, 2025
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132.
Hippo 072 Aspiration System including Cheetah Delivery Tool, REF: AP6072-132.
072 Aspiration Tubing, REF: APT-95
Reason: Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
Root cause: Device Design
Recalling firm: Qapel Medical Inc.Type: Catheter, Thrombus RetrieverDistribution: US: CA, IL, NE, TN, TX, NJ, NC, SD, FL, MI, PA, GA, AL, IN, NY, WI, AZ, MN, LA, OH, OK, SC, NV, ND, ID, MO, CT, WA, MA.
OUS: QATAR, United Arab Emirates, Republic of KazakhstanRecall #Z-1512-2025
Open, ClassifiedPosted Apr 4, 2025·Initiated Feb 21, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows:
CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK, OPEN HEART ADULT PART 1 CDS, OPEN HEART B PACK-LF, OPEN HEART PACK, Z OPEN HEART.
Reason: Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Root cause: Other
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: Cardiovascular Procedure KitDistribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WVRecall #Z-1456-2025
Open, ClassifiedPosted Apr 4, 2025·Initiated Feb 21, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows:
TOL DR R PACK
Reason: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Root cause: Other
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: Laparoscopy KitDistribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WVRecall #Z-1457-2025
Open, ClassifiedPosted Apr 4, 2025·Initiated Feb 21, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows:
HEART BASIN PACK-LF
Reason: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Root cause: Other
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: Kit, Surgical Instrument, DisposableDistribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WVRecall #Z-1458-2025
Open, ClassifiedPosted Apr 4, 2025·Initiated Feb 21, 2025
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows:
CPB ADJUNCT PACK, DR. C PACK, PK CUST CV A&B C CO, TOL DR R PACK, TOL DR. C PACK, TOL DR. M PACK.
Reason: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Root cause: Other
Recalling firm: MEDLINE INDUSTRIES, LP - NorthfieldType: General Surgery TrayDistribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WVRecall #Z-1459-2025
Open, ClassifiedPosted Apr 4, 2025·Initiated Feb 27, 2025
FilmArra Pneumonia Panel plus (Pneumoplus), REF: RFIT-LBL-0374
Reason: Increased risk of control failures and false negative test results with multiplexed nucleic acid test.
Root cause: Nonconforming Material/Component
Recalling firm: BioFire Diagnostics, LLCType: Mers-Cov And Common Respiratory Pathogens Semi-Quantitative And Quantitative Multiplex Nucleic Acid Detection SystemDistribution: OUS International Distribution to countries of: France, Italia, Spain, Switzerland, IsraelRecall #Z-1518-2025
Open, ClassifiedPosted Apr 4, 2025·Initiated Jul 12, 2024
DxI 9000 Access Immunoassay Analyzer, catalog number C11137
in vitro diagnostic
device used for the quantitative, semi-quantitative, or qualitative
determination of various analyte concentrations found in human body
fluids
Reason: Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.
Root cause: Device Design
Recalling firm: Beckman Coulter, Inc.Type: Analyzer, Chemistry (Photometric, Discrete), For Clinical UseDistribution: OUS (Foreign) distribution to countries of: Australia, Croatia, Czechia, France, Germany, Ireland, Israel, Italy, Netherlands, New Zealand, South Africa, Spain, and United
Kingdom of Great Britain and Northern Ireland.Recall #Z-1529-2025