All Non-Sterile Products manufactured by Ameridose LLC — Class II drug recall D-055-2013
Terminated recall by Ameridose LLC, reported 2012-11-21, distributed nationwide. GMP deficiencies
| Recall number | D-055-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ameridose LLC, Westborough, MA, United States |
| Recall initiated | 2012-10-31 |
| Classified | 2012-11-14 |
| Reported by FDA | 2012-11-21 |
| Terminated | 2016-07-25 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
Product
All Non-Sterile Products manufactured by Ameridose LLC, Westborough, MA. A complete list of all products subject to this recall can be accessed on-line at www.ameridose.com
Reason for recall
GMP deficiencies
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-055-2013. 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.