US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 15, 2016 (10 years ago)

Gentell Hydrogel Ag Saturated Gauze

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations

What was recalled

Gentell Hydrogel Ag Saturated Gauze, 2"x2"(NDC 61551-112-20), 4x4(NDC 61554-114-24) and 4"x8"(NDC 61554-118-28), Manufactured by: Gentell, 2701 Bartram Road, Bristol, PA 19007

Recalling firm
Gentell, Inc
NDC code
61551-112-20
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0242-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.