infant product Recalls

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

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

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

Probes may rupture/burst during activation

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.

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.

CheerKid Baby Bath Seats Recalled Due to Drowning Risk

CheerKid recalled baby bath seats on February 12, 2026, due to drowning risks. The seats can tip over, violating safety standards. Parents should stop using them immediately and seek a refund.

Burlington Medical Blockers Recalled for Attenuation Degradation in 51 Units Worldwide (2026)

Potential for attenuation degradation over time, decreasing the lifespan.

Waldemar Link Embrace Drill Tower Recall 74 Units in 2026

The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

Burlington Medical BAT Coverage Recall 1,489 Units Worldwide in 2026

Potential for attenuation degradation over time, decreasing the lifespan.

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Products contain undeclared milk and soy.

Boston Scientific EndoVive PEG Kit Recalled for Sterility Risk in 806 Kits (2026)

International Life Sciences Recalls Artelon FlexBand Dynamic Matrix 31057 for Endotoxin Testing Fail

Augmentation devices failed bacterial endotoxin testing.

International Life Sciences Recalls Artelon FlexBand Plus Augmentation Devices for Endotoxin Testing

Augmentation devices failed bacterial endotoxin testing.

Dresbe LED Christmas Headbands Recalled Over Battery Ingestion Risk (2026)

Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Lack of Assurance of Sterility

Kitosun Submersible LED Lights Recalled Over Battery Ingestion Risk