US Drug Recall Register
Class I · High risk Terminated Initiated Oct 20, 2017 (9 years ago)

diphenoxylate hydrochloride and atropine sulfate tablets, USP, 2.5 mg/0.025 mg, a)…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

SUPERPOTENT: Weight variations resulting in tablets that are sub and super potent

What was recalled

diphenoxylate hydrochloride and atropine sulfate tablets, USP, 2.5 mg/0.025 mg, a) 100-count bottle (NDC 59762-1061-1), b) 1000-count bottle (NDC 59762-1061-2), Rx Only, Distributed by: Greenstone LLC. Peapack, NJ 07977

Recalling firm
Pfizer Inc.
NDC code
59762-1061-1
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0150-2018

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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