cpsc regulated Recalls

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 720G Insulin Pump Recall 2026 Affects 37,458 Units Worldwide

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

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)

Ambrosia Brands Rosabella Moringa Capsules Recalled for Salmonella Contamination (1,224,208 Units)

Product may be contaminated with Salmonella

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

Harbin Jixianglong Biotech Semaglutide Rx Compounding Recall 2026 — 6 Packaging Sizes

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

Erbe USA Recalls 2,408 Flexible Cryoprobes for Surgery Over Rupture Risk (2026)

Probes may rupture/burst during activation

Erbe USA Recalls 5,154 Flexible Cryoprobes for Surgical Use Over Rupture Risk (2026)

Erbe USA recalled 5,154 Flexible Cryoprobes used in surgery after probes may rupture during activation. The defect can cause rupture or burst during activation. Stop using the device and follow recall instructions from the manufacturer.

Olympus OER-Pro Endoscope Reprocessor Recall for 3,354 Units Over MAJ-1443/1444 Compatibility (2026)

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

Erbe USA Recall 33,390 Flexible Cryoprobes Over Rupture Risk (2026)

Probes may rupture/burst during activation

Olympus MAJ-1444 Endoscope Air/Water Valve Recall 2026 for 89,579 Units

The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.