All Non Sterile Products manufactured by NECC — Class II drug recall D-053-2013
Terminated recall by New England Compounding Center, reported 2012-11-21, distributed nationwide. GMP Deviations
| Recall number | D-053-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | New England Compounding Center, Framingham, MA, United States |
| Recall initiated | 2012-10-06 |
| Classified | 2012-11-14 |
| Reported by FDA | 2012-11-21 |
| Terminated | 2016-10-07 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP |
| Reason classes | cgmp |
Product
All Non Sterile Products manufactured by NECC (New England Compounding Center), Framingham, MA. A complete list of products can be found on their website at www.neccrx.com
Reason for recall
GMP Deviations
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-053-2013. 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.