Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as:
1) CANCER SERVICE PORT KIT, Kit SKU DT22710;
2) LINE KIT, Kit SKU DYNDA1857A;
3) PICC REMOVAL KIT, Kit SKU DYNDC1978A;
4) PORT ACCESS TRAY, Kit SKU DYNDC2367;
5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B;
6) CVC DRESSING CHANGE W/ TEG CHG, Kit SKU DYNDC3222A;
7) PICC PROCEDURE PACK, Kit SKU DYNJ59067A;
8) PICC PROCEDURE PACK, Kit SKU PHS950205004B.
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Central Venous Catheter TrayDistribution: US Nationwide distribution.Recall #Z-1329-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
1) UNIVERSAL KIT, Kit SKU DT22010B;
2) VAD ACCESS KIT, Kit SKU DT22790C;
3) VAD ACCESS KIT, Kit SKU DT22790C;
4) PROCEDURE TRAY, Kit SKU DYNDA2966A;
5) PROCEDURE TRAY, Kit SKU DYNDA2966A;
6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C;
7) PORT DRESSING KIT, Kit SKU DYNDC3107;
8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C;
9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250;
10) UMBILICAL VESSEL TRAY, Kit SKU UVT835;
11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: General Surgery TrayDistribution: US Nationwide distribution.Recall #Z-1330-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as:
1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576;
2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Wound Dressing KitDistribution: US Nationwide distribution.Recall #Z-1331-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Suture Removal KitDistribution: US Nationwide distribution.Recall #Z-1332-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Blood And Urine Collection Kit (Excludes Hiv Testing)Distribution: US Nationwide distribution.Recall #Z-1333-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as:
) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C;
2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A;
3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615;
4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660;
5) CENTRAL LINE DRESSING CHANGE K, Kit SKU DT19665;
6) NEONATAL DRESSING CHANGE KIT, Kit SKU DT21495;
7) NICU CVC DRESSING CHANGE TRAY, Kit SKU DT22510A;
8) DRESSING CHANGE TRAY W/TEG CHG, Kit SKU DYNDC3114B;
9) DRESSING CHANGE KIT, Kit SKU DYNDC3351.
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Dressing Change TrayDistribution: US Nationwide distribution.Recall #Z-1334-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Laceration TrayDistribution: US Nationwide distribution.Recall #Z-1335-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Dec 24, 2025
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Reason: Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Root cause: Packaging change control
Recalling firm: Medline Industries, LPType: Circumcision TrayDistribution: US Nationwide distribution.Recall #Z-1336-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Jan 6, 2026
WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM
Reason: The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
Root cause: Under Investigation by firm
Recalling firm: Straumann USA LLCType: Accessories, Implant, Dental, EndosseousDistribution: US Nationwide distribution.Recall #Z-1337-2026
Open, ClassifiedPosted Feb 9, 2026·Initiated Jan 2, 2026
Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Reason: Tyvek bag seal issue which may compromise sterility of the kit.
Root cause: Equipment maintenance
Recalling firm: AVID Medical, Inc.Type: General Surgery TrayDistribution: US Nationwide distribution in the states of New Jersey.Recall #Z-1338-2026
Open, ClassifiedPosted Feb 6, 2026·Initiated Dec 24, 2025
Medline 14 Fr Suction Catheter Kits
SKU DYND40972 - respiratory convenience kit
Reason: A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
Root cause: Under Investigation by firm
Recalling firm: Medline Industries, LPType: Tracheobronchial Suction Catheter KitDistribution: Distribution US nationwide and Canada.Recall #Z-1312-2026
Open, ClassifiedPosted Feb 6, 2026·Initiated Dec 24, 2025
Intubation Tray (Adult) containing Suction Catheter Kits
SKU DYNJAA245B
Reason: A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
Root cause: Under Investigation by firm
Recalling firm: Medline Industries, LPType: Circuit, Breathing (W Connector, Adaptor, Y Piece)Distribution: Distribution US nationwide and Canada.Recall #Z-1313-2026
Open, ClassifiedPosted Feb 6, 2026·Initiated Dec 15, 2025
Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.
Reason: Presence of particulates in affected devices that can be deposited into breast tissue during use.
Root cause: Under Investigation by firm
Recalling firm: Hologic, IncType: Instrument, BiopsyDistribution: US Nationwide distribution.Recall #Z-1314-2026 Open, ClassifiedPosted Feb 6, 2026·Initiated Jan 7, 2026
Brilliance iCT;
Product Code (REF): 728306;
Reason: As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Root cause: Process change control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide - US Nationwide distribution in the states of AL, AR, CA, CO, CT, FL, GA, HI, IL, IN, KY, LA, MA, MD, MN, NC, NY, OH, OR, PA, TX, VT, WA, WV and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Bulgaria, Chile, China, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, France, Germany, Hong Kong, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kuwait, Lithuania, Macao, Mexico, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Russian Fed., Saudi Arabia, Serbia, Singapore, South Africa, South Korea, Spain, Switzerland, Taiwan, Thailand, Turkmenistan, United Kingdom, Uzbekistan, Vietnam.Recall #Z-1315-2026 Open, ClassifiedPosted Feb 6, 2026·Initiated Jan 7, 2026
IQon Spectral CT;
Product Code (REF): 728332;
Reason: As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Root cause: Process change control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide - US Nationwide distribution in the states of AL, AR, CA, CO, CT, FL, GA, HI, IL, IN, KY, LA, MA, MD, MN, NC, NY, OH, OR, PA, TX, VT, WA, WV and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Bulgaria, Chile, China, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, France, Germany, Hong Kong, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kuwait, Lithuania, Macao, Mexico, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Russian Fed., Saudi Arabia, Serbia, Singapore, South Africa, South Korea, Spain, Switzerland, Taiwan, Thailand, Turkmenistan, United Kingdom, Uzbekistan, Vietnam.Recall #Z-1316-2026 Open, ClassifiedPosted Feb 6, 2026·Initiated Jan 7, 2026
Spectral CT;
Product Code (REF): 728333;
Reason: As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Root cause: Process change control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide - US Nationwide distribution in the states of AL, AR, CA, CO, CT, FL, GA, HI, IL, IN, KY, LA, MA, MD, MN, NC, NY, OH, OR, PA, TX, VT, WA, WV and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Bulgaria, Chile, China, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, France, Germany, Hong Kong, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kuwait, Lithuania, Macao, Mexico, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Russian Fed., Saudi Arabia, Serbia, Singapore, South Africa, South Korea, Spain, Switzerland, Taiwan, Thailand, Turkmenistan, United Kingdom, Uzbekistan, Vietnam.Recall #Z-1317-2026 Open, ClassifiedPosted Feb 6, 2026·Initiated Jan 7, 2026
Spectral CT 7500 on Rails;
Product Code (REF): 728334;
Reason: As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Root cause: Process change control
Recalling firm: Philips North America LlcType: System, X-Ray, Tomography, ComputedDistribution: Worldwide - US Nationwide distribution in the states of AL, AR, CA, CO, CT, FL, GA, HI, IL, IN, KY, LA, MA, MD, MN, NC, NY, OH, OR, PA, TX, VT, WA, WV and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Bulgaria, Chile, China, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, France, Germany, Hong Kong, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kuwait, Lithuania, Macao, Mexico, Netherlands, New Zealand, Norway, Panama, Philippines, Poland, Portugal, R¿union, Russian Fed., Saudi Arabia, Serbia, Singapore, South Africa, South Korea, Spain, Switzerland, Taiwan, Thailand, Turkmenistan, United Kingdom, Uzbekistan, Vietnam.Recall #Z-1318-2026 Open, ClassifiedPosted Feb 6, 2026·Initiated Dec 22, 2025
Medline ReNewal Reprocessed Webster CS Catheters:
Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer
BD710DF282CRH;
Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer
BD710DF282RRH
BD710FJ282RRH;
Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/AutoID w/ EZ Steer
BD710FJ282CRH;
Reason: These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
Root cause: Under Investigation by firm
Recalling firm: Medline Industries, LPType: Catheter, Recording, Electrode, ReprocessedDistribution: Distribution US nationwide.Recall #Z-1319-2026
Open, ClassifiedPosted Feb 6, 2026·Initiated Dec 22, 2025
Reprocessed Abbott Inquiry Steerable Diagnostic Catheters:
Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm
81105RH
81172RH;
Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm
81202RH;
Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm
81483RH;
Inquiry Steerable
Diagnostic Catheter 10
Elec. 2-5-2mm
81102RH
81104RH
81174RH
81531RH
81532RH;
Inquiry Steerable
Diagnostic Catheter 10
Elec. 5mm
81107RH;
Inquiry Steerable
Diagnostic Catheter 4
Elec. 2-5-2mm
81402RH
81404RH
81405RH
81474RH;
Inquiry Steerable
Diagnostic Catheter 4
Elec. 5mm
81473RH
Reason: These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
Root cause: Under Investigation by firm
Recalling firm: Medline Industries, LPType: Catheter, Recording, Electrode, ReprocessedDistribution: Distribution US nationwide.Recall #Z-1320-2026
Open, ClassifiedPosted Feb 6, 2026·Initiated Dec 22, 2025
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters:
Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm
401582RH
401940RH;
Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm
401904RH;
Livewire Steerable Electrophysiology Catheter,20 Elec. 2-5-2mm
401914RH;
Livewire Steerable Electrophysiology Catheter,20 Elec. 2-8-2-60-2-8-2mm
401932RH;
Livewire Steerable Electrophysiology Catheter,8 Elec. 2-2-2mm
401652RH;
Reason: These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
Root cause: Under Investigation by firm
Recalling firm: Medline Industries, LPType: Catheter, Recording, Electrode, ReprocessedDistribution: Distribution US nationwide.Recall #Z-1321-2026