Flanax — Class III drug recall D-136-2013
Terminated recall by Belmora LLC, reported 2013-01-30, distributed nationwide. Defective Container: Product lacks tamper evident breakaway band on cap.
| Recall number | D-136-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Belmora LLC, Arlington, VA, United States |
| Recall initiated | 2012-12-18 |
| Classified | 2013-01-24 |
| Reported by FDA | 2013-01-30 |
| Terminated | 2013-04-05 |
| Distributed | Nationwide (US) |
| Quantity | 17,996 bottles |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00853030002090 |
| Lot numbers | 1321, 1322, 1323, 1324 |
Product
Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.
Reason for recall
Defective Container: Product lacks tamper evident breakaway band on cap.
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-136-2013. 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.