Home › Drive Devilbiss Healthcare › Hugo

Hugo

Drive Devilbiss Healthcare · Model 727-180 · UDI-DI 07540212109540

IPR Prescription

510(k) clearances

522

Adverse events

Recalls

194

Facilities

Description

HUGO CR. PADS, 1PR,6PR/CV,72PR/CT,Ret

Recalls

Date	Firm	Reason
2004-08-04	Duro-Med Industries, Inc.	The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04	Duro-Med Industries, Inc.	The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04	Duro-Med Industries, Inc.	The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04	Duro-Med Industries, Inc.	The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
2004-08-04	Duro-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 key Read 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.