FDA Drug recall D-055-2013
All Non-Sterile Products manufactured by Ameridose LLC, Westborough, MA. A complete list of all products subject to this recall can be acce…
- FDA Drug
- Class II
- terminated
- Published 2012-11-21
On 2012-11-21 the FDA classified a Class II recall of All Non-Sterile Products manufactured by Ameridose LLC, Westborough, MA. A complete list of all products subject to this recall can be acce… by Ameridose, citing GMP deficiencies.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-055-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-10-31 |
| Published | 2012-11-21 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Ameridose |
| Distribution | US |
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
GMP deficiencies
Identifiers
| code_info | All lot codes within expiry |
|---|
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-055-2013%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.