RecallWatchMedical Device Safety

Sitemap

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

20261,658 20252,908

Why it was recalled

By root cause

Under Investigation by firm1,121 Process control816 Device Design588 Nonconforming Material/Component386 Software design262 No Marketing Application228 Process change control185 Process design86 Component design/selection82 Package design/selection68 Labeling Change Control66 Other61 Component change control48 Labeling design47 Radiation Control for Health and Safety Act45 Use error44

Recalling firm

By manufacturer

Medline Industries, LP457 Olympus Corporation of the Americas163 MEDLINE INDUSTRIES, LP - Northfield161 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.157 B Braun Medical Inc137 Boston Scientific Corporation111 Philips Ultrasound, Inc101 GET TESTED INTERNATIONAL AB92 Baxter Healthcare Corporation81 GE Medical Systems, LLC76 Philips North America Llc74 Philips North America64 Intuitive Surgical, Inc.56 ICU Medical, Inc.55 CareFusion 303, Inc.52 AVID Medical, Inc.52 ARROW INTERNATIONAL, LLC47 SEDECAL SA46