Medical Device Recalls

FDA alerts on implants, diagnostic equipment, and life-sustaining devices. Know the risks to your health.

CriticalMar 1, 2026

Medtronic Recalls 45,000 Heart Devices Over Battery Failure Risk

Implantable cardiac defibrillators may experience unexpected battery depletion, potentially causing life-threatening failures.

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CriticalFeb 25, 2026

Philips Expands CPAP Recall to Additional 2 Million Devices

Sound abatement foam degradation may release toxic particles and gases into the air pathway of affected machines.

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CriticalFeb 18, 2026

Abbott Recalls FreeStyle Libre 3 Sensors for Inaccurate Readings

Certain sensor lots may provide falsely low glucose readings, potentially leading to incorrect insulin dosing.

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WarningFeb 12, 2026

Stryker Issues Voluntary Recall on Hip Replacement Components

Increased reports of early component wear may lead to metal debris release and tissue damage requiring revision surgery.

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WarningFeb 6, 2026

Baxter Recalls IV Pump Software Due to Dosing Calculation Errors

A software bug in certain infusion pumps may result in incorrect medication delivery rates in hospital settings.

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