Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed 740G Insulin Pump Recalled for 24,946 Units Worldwide (2026)
Medtronic MiniMed
All Medtronic
electronic Recalls
325 recalls tagged with “electronic”.
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed Paradigm Revel Insulin Pumps Recalled: 26,647 Units Worldwide (2026)
Medtronic MiniMed
All Medtronic
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed 720G Insulin Pump Recall 2026 Affects 37,458 Units Worldwide
Medtronic MiniMed
All Medtronic
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed Paradigm Veo Insulin Pump Recalled for 55,724 Units (2026)
Medtronic MiniMed
All Medtronic
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed Recalled 116,645 Insulin Pumps Over Delivery Risk (2026)
Medtronic MiniMed
All Medtronic
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed 700G Insulin Pump Recalled for Insulin Delivery Errors (13,811 Units, 2026)
Medtronic MiniMed
All Medtronic
Health & Personal Care
HIGH
FDA DEVICE
Medtronic MiniMed 630G Insulin Pumps Recalled in 2026 for Insulin Delivery Errors (60,880 Units)
Medtronic MiniMed
All Medtronic
Health & Personal Care
HIGH
FDA DEVICE
Erbe USA Recalls 2,408 Flexible Cryoprobes for Surgery Over Rupture Risk (2026)
Probes may rupture/burst during activation
Erbe USA
Probes
Health & Personal Care
HIGH
FDA DEVICE
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.
Erbe USA
Probes
Health & Personal Care
HIGH
FDA DEVICE
Olympus Endoscope Reprocessor OER-Elite Recall Affects 2,929 Units (2026)
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.
Olympus Corporation of the Americas
The MAJ-1443
Health & Personal Care
HIGH
FDA DEVICE
Erbe USA Recall 33,390 Flexible Cryoprobes Over Rupture Risk (2026)
Probes may rupture/burst during activation
Erbe USA
Probes
Health & Personal Care
HIGH
FDA DEVICE
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.
Olympus Corporation of the Americas
The MAJ-1443
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 BD Alaris System with Guardrails Suite MX Recall Impacts 1,025,567 Units (2026)
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
CareFusion 303
Due to
Health & Personal Care
HIGH
FDA DEVICE
Burlington Medical Half Aprons Recalled for Attenuation Degradation Risk (2026)
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Burlington Medical BAT Coverage Recall 1,489 Units Worldwide in 2026
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Burlington Medical Recalls 961 Caps for Medical Devices Over Attenuation Degradation (2026)
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Burlington Medical Thyroid Shield Recall 2026 Affects 41,962 Units Worldwide
Potential for attenuation degradation over time, decreasing the lifespan.
Burlington Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)
Reflexion Medical
Due to
Health & Personal Care
HIGH
FDA DEVICE
BD Kiestra ReadA Lab Automation Module Recalled in 2026 Over Connectivity Delays (82 Units)
BD Kiestra Lab Automation
In certain
Health & Personal Care
HIGH
FDA DEVICE
Trividia Health TRUE METRIX PRO Owner's Booklet Recall for 1,001,534 Units (2026)
Trividia Health
The system