FDA Drug recall D-1056-2017
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
- FDA Drug
- Class II
- terminated
- Published 2017-08-09
On 2017-08-09 the FDA classified a Class II recall of Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60 by Teva Pharmaceuticals Usa, citing failed Tablet/Capsule Specification; out of specification for tablet weight.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1056-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-24 |
| Published | 2017-08-09 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Teva Pharmaceuticals Usa |
| Distribution | US |
Product
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
Reason
Failed Tablet/Capsule Specification; out of specification for tablet weight
Identifiers
| ndc | 0172-5728-60 |
|---|---|
| ndc | 0172-5728-70 |
| ndc | 0172-5728-80 |
| ndc | 0172-5729-60 |
| ndc | 0172-5729-70 |
| code_info | Lot # 3429066, exp 06/2018 |
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-1056-2017%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.