FDA Device Intelligence
HomeDrive Devilbiss Healthcare › DRIVEMEDICAL

DRIVEMEDICAL

Drive Devilbiss Healthcare · Model 10400-8 · UDI-DI 50822383101533

IPR
4
510(k) clearances
373
Adverse events
5
Recalls
194
Facilities

Description

Canes & CrutchesCrutches Product Description: Crutch, Adult, 8pr/cs

Recalls

DateFirmReason
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.
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.