FDA Drug recall D-136-2013
Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Dist…
- FDA Drug
- Class III
- terminated
- Published 2013-01-30
On 2013-01-30 the FDA classified a Class III recall of Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Dist… by Belmora, citing defective Container: Product lacks tamper evident breakaway band on cap.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-136-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2012-12-18 |
| Published | 2013-01-30 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Belmora |
| Distribution | US |
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
Defective Container: Product lacks tamper evident breakaway band on cap.
Identifiers
| upc | 853030002090 |
|---|---|
| code_info | Lot #: 1321, 1322, 1323, and 1324 |
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-136-2013%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.