FDA Device Intelligence
HomeThermor Ltd › BIOS Living

BIOS Living

Thermor Ltd · Model 56033 · UDI-DI 00057475560331

INP
8
510(k) clearances
339
Adverse events
9
Recalls
143
Facilities

Description

Walker Skiis

Recalls

DateFirmReason
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2016-02-17Medical Depot Inc.Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
2004-08-04Duro-Med Industries, Inc.The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04Duro-Med Industries, Inc.The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04Duro-Med Industries, Inc.The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.