RecallRadar

FDA Drug recall D-0652-2017

Penicillin V Potassium Tablets, USP 500 mg (800,000 units) 1000 count bottles, Rx Only, Distributed by: Citron Pharma LLC, East Brunswick,…

On 2017-04-19 the FDA classified a Class III recall of Penicillin V Potassium Tablets, USP 500 mg (800,000 units) 1000 count bottles, Rx Only, Distributed by: Citron Pharma LLC, East Brunswick,… by Citron Pharma, citing presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0652-2017
ClassificationClass III
Statusterminated
Initiated2017-02-24
Published2017-04-19
Last updated2026-09-13 11:51 UTC
CompanyCitron Pharma
DistributionUS

Product

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

Reason

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

Identifiers

ndc57237-040-01
ndc57237-040-99
ndc57237-041-01
ndc57237-041-05
ndc57237-041-99
code_infoBatch Numbers: PE5015069-A, exp 11/2018

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0652-2017%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.