HYDROXYPROGESTERONE CAPROATE 250 MG/ML — Class II drug recall D-0016-2014
Terminated recall by Avella of Deer Valley, Inc., reported 2014-10-22, distributed nationwide. Crystallization: Formation of crystals observed in product.
| Recall number | D-0016-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Avella of Deer Valley, Inc., Phoenix, AZ, United States |
| Recall initiated | 2014-10-01 |
| Classified | 2014-10-10 |
| Reported by FDA | 2014-10-22 |
| Terminated | 2015-02-20 |
| Distributed | Nationwide (US) |
| Quantity | 197 vials |
| Lot numbers | 01/15, 12/14 |
Product
HYDROXYPROGESTERONE CAPROATE 250 MG/ML (IN SESAME OIL), Rx Only 4 mL INJECTABLE IM USE. Manufactured by Avella Specialty Pharmacy, Phoenix, AZ 85085.
Reason for recall
Crystallization: Formation of crystals observed in product.
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-0016-2014. 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.