RecallWatchMedical Device Safety

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Browse recall categories

Every recall, organized by the dimensions that matter — severity, when it was reported, where it was distributed, and who made the device.

Risk level

By severity

Most serious — risk of serious injury or death

Temporary or reversible health consequences

Unlikely to cause adverse health consequences

Reported

By year

20262,024 20252,908

Why it was recalled

By root cause

Under Investigation by firm1,228 Process control853 Device Design620 Nonconforming Material/Component426 Software design278 No Marketing Application229 Process change control212 Process design95 Component design/selection88 Labeling Change Control78 Package design/selection68 Material/Component Contamination63 Other61 Radiation Control for Health and Safety Act53 Labeling design49 Component change control49

Recalling firm

By manufacturer

Medline Industries, LP503 Olympus Corporation of the Americas171 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.163 MEDLINE INDUSTRIES, LP - Northfield161 B Braun Medical Inc137 Boston Scientific Corporation128 Philips Ultrasound, Inc101 GET TESTED INTERNATIONAL AB92 Baxter Healthcare Corporation82 GE Medical Systems, LLC79 Philips North America Llc76 AVID Medical, Inc.65 Philips North America64 Intuitive Surgical, Inc.57 ICU Medical, Inc.57 CareFusion 303, Inc.52 American Contract Systems Inc49 Cardinal Health 200, LLC48