Data Foundry

Drug recalls 2017

Penicillin V Potassium Tablets — Class III drug recall D-0652-2017

Terminated recall by Citron Pharma Llc, reported 2017-04-19, distributed nationwide. Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg

Recall numberD-0652-2017
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCitron Pharma Llc, East Brunswick, NJ, United States
Recall initiated2017-02-24
Classified2017-04-07
Reported by FDA2017-04-19
Terminated2019-09-09
DistributedNationwide (US)
Quantity420 bottles
NDC57237-0040, 57237-0040-01, 57237-0040-99, 57237-0041, 57237-0041-01, 57237-0041-05, 57237-0041-99
Lot numbersPE5015069-A
Expiration dates2018-11

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 for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0652-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.