Altrenogest 50 mg/ml Injection — Class II drug recall D-696-2013
Ongoing recall by Lowlite Investments, Inc. D/B/A Olympia Pharmacy, reported 2013-07-17, distributed nationwide. Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control process
| Recall number | D-696-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lowlite Investments, Inc. D/B/A Olympia Pharmacy, Orlando, FL, United States |
| Recall initiated | 2013-05-29 |
| Classified | 2013-07-11 |
| Reported by FDA | 2013-07-17 |
| Distributed | Nationwide (US) |
| Quantity | 1 |
| Reason classes | sterility |
| Expiration dates | 2013-11-30 |
Product
Altrenogest 50 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL
Reason for recall
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Machine access
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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.