Open, ClassifiedPosted May 22, 2026·Initiated Apr 13, 2026
Halyard Purezero Ultraviolet Nitrile Exam Gloves
Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
Reason: Nitrile Exam Glove failed to meet specifications chemical permeation performance.
Root cause: Under Investigation by firm
Recalling firm: O&M HALYARD INCType: Medical Glove, SpecialtyDistribution: US Nationwide distribution in the states of GA, CA, NJ, MA, NY, NC.Recall #Z-2230-2026
Open, ClassifiedPosted May 21, 2026·Initiated Apr 28, 2026
Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers.
1. Azurion 3 M12; Model Numbers: 722063, 722229.
2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230.
3. Azurion 5 M12; Model Numbers: 722227, 722231.
4. Azurion 5 M20; Model Numbers: 722228, 722232, 722281.
5. Azurion 7 B12; Model Numbers: 722067, 722225, 722235.
6. Azurion 7 B20; Model Numbers: 722068, 722226, 722236.
7. Azurion 7 M12; Model Numbers: 722078, 722223, 722233.
8. Azurion 7 M20; Model Numbers: 722079, 722224, 722234, 722282.
Reason: Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.
Root cause: Device Design
Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Type: Interventional Fluoroscopic X-Ray SystemDistribution: Nationwide distribution. International distribution to Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Canada, Chile, C¿te D'Ivoire, El Salvador, Estonia, Greece, Honduras, Hong Kong, Iceland, Indonesia, Iraq, Japan, Kyrgyzstan, Malaysia, Malta, Moldova, Nepal, New Zealand, Philippines, Qatar, Singapore, South Africa, Sri Lanka, Syrian Arab Republic, Tanzania, Turkmenistan, Vietnam, YemenRecall #Z-2225-2026
Open, ClassifiedPosted May 21, 2026·Initiated Apr 23, 2026
Silastic Foley Catheters
Silastic Brand Foley Catheter 30cc
REF:
33416
33418
33420
33422
33424
Silastic Brand Foley Catheter 5cc
REF:
33614
33616
33618
33620
33622
33624
Reason: Due to stain present on the surface of affected foley catheters.
Root cause: Material/Component Contamination
Recalling firm: C.R. Bard IncType: Catheter, Retention Type, BalloonDistribution: U.S.: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI
O.U.S.: CanadaRecall #Z-2226-2026
Open, ClassifiedPosted May 21, 2026·Initiated Apr 28, 2026
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
Reason: The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage.
Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a
certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message
Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by
restarting the system.
Root cause: Component design/selection
Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Type: Interventional Fluoroscopic X-Ray SystemDistribution: Domestic: Nationwide;
International: Canada, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Malta, Martinique, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, Yemen;Recall #Z-2227-2026
Open, ClassifiedPosted May 21, 2026·Initiated Apr 28, 2026
Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20 Biplane OR Table (722025), Allura Xper FD20/10 (722029), Allura Xper FD20/15 (722058), Allura Xper FD20/15 OR Table (722059), Allura Xper FD20/20 (722038), Allura Xper FD20/20 OR Table (722039), Cardio Vascular-Allura (722400);
Reason: The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage.
Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a
certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message
Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by
restarting the system.
Root cause: Component design/selection
Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Type: Interventional Fluoroscopic X-Ray SystemDistribution: Domestic: Nationwide;
International: Canada, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Malta, Martinique, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, Yemen;
Open, ClassifiedPosted May 21, 2026·Initiated Apr 28, 2026
Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV Cesar-Powerpack (722030), Integris H5000 C / Allura 9C (722016);
Reason: The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage.
Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a
certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message
Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by
restarting the system.
Root cause: Component design/selection
Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Type: Interventional Fluoroscopic X-Ray SystemDistribution: Domestic: Nationwide;
International: Canada, Algeria, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, French Polynesia, Georgia, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Malaysia, Maldives, Malta, Martinique, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Viet Nam, Yemen;Recall #Z-2229-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 23, 2026
OneLIF Interbody Cage (REF/Description):
010-107-1007/Small 7 Degree 10mm X 7mm,
010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique,
010-107-1209/Small 7 Degree 12mm X 9mm,
010-107-1411/Small 7 Degree 14mm X 11mm,
010-107-1613/Small 7 Degree 16mm X 13mm,
010-113-1006/Small, 13 Degree 10mm X 6mm,
010-113-1006-2/Small, 13 Degree, 10mm X 6mm - Oblique,
010-113-1208/Small 13 Degree 12mm X 8mm,
010-113-1410/Small 13 Degree 14mm X 10mm,
010-113-1612/Small 13 Degree 16mm X 12mm,
010-119-1407/19 Degree 14mm X 7mm,
010-119-1609/Small 19 Degree 16mm X 9mm,
010-119-1811/Small 19 Degree 18mm X 11mm,
010-125-1606/Small 25 Degree 16mm X 6mm,
010-125-1808/Small 25 Degree 18mm X 8mm,
010-207-1007/Medium 7 Degree 10mm X 7mm,
010-207-1007-2/Medium 7 Degree 10mm X 7mm - Oblique,
010-207-1209/Medium 7 Degree 12mm X 9mm,
010-207-1411/Medium 7 Degree 14mm X 11mm,
010-207-1613/Medium 7 Degree 16mm X 13mm,
010-213-1206/Medium 13 Degree 12mm X 6mm,
010-213-1408/Medium 13 Degree 14mm X 8mm,
010-213-1610/Medium 13 Degree 16mm X 10mm,
010-213-1812/Medium 13 Degree 18mm X 12mm,
010-219-1406/Medium 19 Degree 14mm X 6mm,
010-219-1608/Medium 19 Degree 16mm X 8mm,
010-219-1810/Medium 19 Degree 18mm X 10mm,
010-225-1807/Medium 25 Degree 18mm X 7mm,
010-225-2009/Medium 25 Degree 20mm X 9mm,
010-307-1006/Large 7 Degree,10mm X 6mm,
010-307-1006-2/Large 7 Degree 10mm X 6mm - Oblique,
010-307-1208/ Large 7 Degree 12mm X 8mm,
010-307-1410/Large 7 Degree 14mm X 10mm,
010-307-1612/Large 7 Degree 16mm X 12mm,
010-313-1205/Large 13 Degree 12mm X 5mm,
010-313-1407/Large 13 Degree 14mm X 7mm,
010-313-1609/Large 13 Degree 16mm X 9mm,
010-313-1811/Large 13 Degree 18mm X 11mm,
010-313-2013/Large 13 Degree 20mm X 13mm,
010-319-1606/Large 19 Degree 16mm X 6mm,
010-319-1808/ Large 19 Degree 18mm X 8mm,
010-319-2010/ Large 19 Degree 20mm X 10mm,
010-325-2007/Large 25 Degree 20mm X 7mm,
010-325-2209/ Large 25 Degree 22mm X 9mm,
Implant Kits containing OneLIF Interbody Cages, Name/Kit Family:
Kit-OneLIF-10 mm (716)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (717)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (718)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (719)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (722)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (723)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (724)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (733)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (734)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (737)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (738)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (746)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (751)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (761)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (762)/Kit-OneLIF-10 mm,
Kit-OneLIF-10 mm (787)/Kit-OneLIF-10 mm,
Kit-OneLIF- IMPOneLIF Implant Kit (701)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (702)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (703) NL/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (704)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (705)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (706)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (708)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Kit-OneLIF-IMP - OneLIF Implant Kit (709)/Kit-OneLIF-IMP - OneLIF Implant Kit,
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2214-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2215-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2216-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2217-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2218-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2219-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2220-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2221-2026
Open, ClassifiedPosted May 20, 2026·Initiated Apr 21, 2026
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular catheter
Reason: Certain lots of product have the potential for a sterile barrier breach.
Root cause: Packaging process control
Recalling firm: Medtronic Perfusion SystemsType: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary BypassDistribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, China, Colombia, Costa Rica, Cyprus, Denmark, France, Germany, Hong Kong, Hungary, Italy, Japan, Latvia, Lithuania, Malaysia, Moldova, Republic Of, Morocco, Netherlands, Norway, Panama, Poland, Russia, Serbia, Singapore, South Africa, South Korea, Spain, Suriname, Sweden, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, United States, Uruguay, Vietnam.Recall #Z-2222-2026
Open, ClassifiedPosted May 18, 2026·Initiated Mar 24, 2026
Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960
Reason: Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption with the potential for the patient to receive less infusion solution than intended. Exposure of hazardous substances to the patient, caregiver, or pharmacy technician is possible.
Root cause: Process control
Recalling firm: ICU Medical, Inc.Type: Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemDistribution: US Nationwide distribution in the states of GA, MA, OH, NC, CA, ND, MI, TX, FL, AR, CT, PA, WA, WI, CO, VT, NY, NH, KY, IA, KS, AL, NM, IL, MO, NJ.Recall #Z-2210-2026
Open, ClassifiedPosted May 15, 2026·Initiated Apr 8, 2026
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
Reason: Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Root cause: Process change control
Recalling firm: Becton, Dickinson and CompanyType: Introducer, CatheterDistribution: Worldwide - US Nationwide distribution including in the states of TX, SC, CT, GA, VA, MO, NM, UT, NJ, CA, FL, PA, IN, TN, WA, KY, MD, WV, MI, MA, NC, MN, NY, AZ, AL, LA, CO, OK, HI, MS, IL, OH, NE, DC, KS, NV, WI, SD, IA, AR, ID, OR, WY, MT, RI, VT, DE, AK, NH, ND, ME, PR and the countries of Japan, Brazil, Colombia, Australia, New Zealand, Poland, Czech Republic, South Africa, Mauritius, Germany, Israel, Iran, Slovakia, Switzerland, Slovenia, Bulgaria, Cyprus, Saudi Arabia, United Arab Emirates (UAE), Kuwait, Malta, Bahrain, Qatar, Hungary, Morocco, Romania, Lebanon, Tunisia, Oman, Turkey, Austria, Belgium, Luxembourg, France, Netherlands, Italy, Spain, Canary Islands, Portugal, United Kingdom, Northern Ireland, Ireland, Denmark, Sweden, Iceland, Norway, Estonia, Finland, Greece, Chile, Puerto Rico, Canada.Recall #Z-2202-2026
Open, ClassifiedPosted May 15, 2026·Initiated Apr 8, 2026
Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
Reason: Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Root cause: Process change control
Recalling firm: Becton, Dickinson and CompanyType: Catheter, Flow DirectedDistribution: Worldwide - US Nationwide distribution including in the states of TX, SC, CT, GA, VA, MO, NM, UT, NJ, CA, FL, PA, IN, TN, WA, KY, MD, WV, MI, MA, NC, MN, NY, AZ, AL, LA, CO, OK, HI, MS, IL, OH, NE, DC, KS, NV, WI, SD, IA, AR, ID, OR, WY, MT, RI, VT, DE, AK, NH, ND, ME, PR and the countries of Japan, Brazil, Colombia, Australia, New Zealand, Poland, Czech Republic, South Africa, Mauritius, Germany, Israel, Iran, Slovakia, Switzerland, Slovenia, Bulgaria, Cyprus, Saudi Arabia, United Arab Emirates (UAE), Kuwait, Malta, Bahrain, Qatar, Hungary, Morocco, Romania, Lebanon, Tunisia, Oman, Turkey, Austria, Belgium, Luxembourg, France, Netherlands, Italy, Spain, Canary Islands, Portugal, United Kingdom, Northern Ireland, Ireland, Denmark, Sweden, Iceland, Norway, Estonia, Finland, Greece, Chile, Puerto Rico, Canada.Recall #Z-2203-2026
Open, ClassifiedPosted May 15, 2026·Initiated Apr 8, 2026
Swan-Ganz Pacing Catheter, Models: D200F7;
Reason: Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Root cause: Process change control
Recalling firm: Becton, Dickinson and CompanyType: Catheter, Flow DirectedDistribution: Worldwide - US Nationwide distribution including in the states of TX, SC, CT, GA, VA, MO, NM, UT, NJ, CA, FL, PA, IN, TN, WA, KY, MD, WV, MI, MA, NC, MN, NY, AZ, AL, LA, CO, OK, HI, MS, IL, OH, NE, DC, KS, NV, WI, SD, IA, AR, ID, OR, WY, MT, RI, VT, DE, AK, NH, ND, ME, PR and the countries of Japan, Brazil, Colombia, Australia, New Zealand, Poland, Czech Republic, South Africa, Mauritius, Germany, Israel, Iran, Slovakia, Switzerland, Slovenia, Bulgaria, Cyprus, Saudi Arabia, United Arab Emirates (UAE), Kuwait, Malta, Bahrain, Qatar, Hungary, Morocco, Romania, Lebanon, Tunisia, Oman, Turkey, Austria, Belgium, Luxembourg, France, Netherlands, Italy, Spain, Canary Islands, Portugal, United Kingdom, Northern Ireland, Ireland, Denmark, Sweden, Iceland, Norway, Estonia, Finland, Greece, Chile, Puerto Rico, Canada.Recall #Z-2204-2026