replacement available Recalls

Medline recalls 14,379 Olympus biopsy valve kits over rubber fragments in 2026 recall

Olympus Biopsy Valves in Medline Thoracic Robotic Kits Recalled for Rubber Fragments (14,379 Kits,

Medline Recalls 14,379 Olympus Biopsy Valve Kits in 2026

Merit Medical CentrosFLO Hemodialysis Catheters Recalled for 35,591 Units (2026)

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, and procedure delay.

Merit Medical 16F Dual-Valved Splittable Sheath Introducer Recalled for 368,264 Units Worldwide (202

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, and procedure delay.

Medtronic MiniMed 530G Insulin Pumps Recalled for Delivery Errors in 2026 (13,429 Units)

Merit Medical's DuraMax 16F Hemodialysis Catheter Recalled For Splittable Sheath Defect (2026)

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, and procedure delay.

Medline ENFIT G-Tube Connector ENFIT1010GC Recalled for Leakage Risk (651,789 Units, 2026)

Medtronic MiniMed 740G Insulin Pump Recalled for 24,946 Units Worldwide (2026)

Medtronic MiniMed Paradigm Revel Insulin Pumps Recalled: 26,647 Units Worldwide (2026)

Medtronic MiniMed Paradigm Veo Insulin Pump Recalled for 55,724 Units (2026)

Merit Medical ProGuide 16F Dialysis Sheath Introducer Recalled Worldwide in 2026 (131 Units)

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, and procedure delay.

Merit Medical BioFlo DuraMax Catheter Recall 2026: 47,153 Units Worldwide

16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, and procedure delay.

Medtronic MiniMed 620G Insulin Pump Recall Impacts 799 Units Worldwide (2026)

Medtronic MiniMed 700G Insulin Pump Recalled for Insulin Delivery Errors (13,811 Units, 2026)

Medtronic MiniMed Paradigm Real-Time Insulin Pump Recalled for 29,074 Units Worldwide (2026)

Medline ENFIT G-Tube Connector Kits Recalled for Leakage Risk in 2026

Medtronic MiniMed 630G Insulin Pumps Recalled in 2026 for Insulin Delivery Errors (60,880 Units)

Medtronic MiniMed 770G Insulin Pump Recall Affects 95,704 Units Worldwide (2026)

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall (2026)

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution