US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 29, 2021 (5 years ago)

PAIN AID ESF- (Acetaminopehn USP 250mg, Asprin USP 250mg Caffeine 65mg) coated, bulk OTC…

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

Why it was recalled

CGMP Deviations: failed stability results, inadequate laboratory investigations,

What was recalled

PAIN AID ESF- (Acetaminopehn USP 250mg, Asprin USP 250mg Caffeine 65mg) coated, bulk OTC tablets packaged in corrugated boxes lined with 2 polyethylene bags 100 lb, ULTRAtab Laboratories, Inc. NDC# 62959-560-00, Product Code M560L

Recalling firm
ULTRAtab Laboratories, Inc.
NDC code
62959-560-00
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0327-2022

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.

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