US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 24, 2017 (10 years ago)

Penicillin V Potassium Tablets, USP 500 mg (800,000 units) 1000 count bottles, Rx Only…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg

What was recalled

Penicillin V Potassium Tablets, USP 500 mg (800,000 units) 1000 count bottles, Rx Only, Distributed by: Citron Pharma LLC, East Brunswick, NJ --- NDC 57237-041-99

Recalling firm
Citron Pharma Llc
NDC code
57237-041-99
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0652-2017

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.

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