Baclofen USP powder — Class II drug recall D-0573-2016
Terminated recall by Freedom Pharmaceuticals Inc, reported 2016-01-27, distributed nationwide. Presence of Foreign Substance
| Recall number | D-0573-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Freedom Pharmaceuticals Inc, Broken Arrow, OK, United States |
| Recall initiated | 2015-11-09 |
| Classified | 2016-01-19 |
| Reported by FDA | 2016-01-27 |
| Terminated | 2016-12-23 |
| Distributed | Nationwide (US) |
| NDC | 52372-0909-01, 52372-0909-10, 52372-0909-25, 52372-0909-50 |
| Lot numbers | F10867, F10867A, F10918, F10918-2 |
| Expiration dates | 2016-03-11, 2016-07-24 |
Product
Baclofen USP powder, packaged in (a) 25gm (4 oz container), (b) 100gm (16 oz container), (c) 500 gm (70 oz container), and (d) 1000 gm (120 oz container, Rx only, 801 W New Orleans St. Broken Arrow, OK 74011. NDC: (a) 52372-0909-25; (b) 52372-0909-01; (c) 52372-0909-50; (d) 52372-0909-10.
Reason for recall
Presence of Foreign Substance
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-0573-2016. 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.