Ciprofloxacin Tablets — Class III drug recall D-1422-2012
Terminated recall by Pack Pharmaceuticals, reported 2012-07-25, distributed nationwide. Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initia
| Recall number | D-1422-2012 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pack Pharmaceuticals, Buffalo Grove, IL, United States |
| Recall initiated | 2012-03-09 |
| Classified | 2012-07-19 |
| Reported by FDA | 2012-07-25 |
| Terminated | 2012-07-19 |
| Distributed | Nationwide (US) |
| Quantity | 4,848 bottles |
| Reason classes | labeling |
| NDC | 16571-0411, 16571-0411-10, 16571-0412, 16571-0412-10, 16571-0412-50, 16571-0413, 16571-0413-05 |
| Lot numbers | PUB1040 |
| Expiration dates | 2015-08 |
Product
Ciprofloxacin Tablets, USP, 500 mg, Rx Only, 100 Tablets per Bottle, Manufactured in India by: Unique Pharmaceutical Laboratories (A Division of J.B. Chemicals & Pharmaceuticals Ltd.), Mumbai - 400 030, Distributed by: PACK Pharmaceuticals, LLC, Buffalo Grove, IL 60089, NDC 16571-412-10.
Reason for recall
Labeling Illegible: Missing Label; The voluntary recall of the aforementioned batch of product is being initiated due to two bottles missing container labels.
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-1422-2012. 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.