All Sterile Products manufactured by Ameridose LLC — Class II drug recall D-054-2013
Terminated recall by Ameridose LLC, reported 2012-11-21, distributed nationwide. Lack of assurance of sterility
| Recall number | D-054-2013 |
|---|---|
| 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 | sterility |
Product
All 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
Lack of assurance of sterility
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-054-2013. 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.