Fludeoxyglucose F 18 Injection USP — Class II drug recall D-579-2013
Terminated recall by Petnet Solution Inc, reported 2013-06-12, distributed in CA. cGMP Deviation
| Recall number | D-579-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Petnet Solution Inc, Irvine, CA, United States |
| Recall initiated | 2013-02-22 |
| Classified | 2013-06-06 |
| Reported by FDA | 2013-06-12 |
| Terminated | 2013-06-06 |
| Distributed | CA |
| Quantity | 28 doses |
| Reason classes | cgmp |
| Lot numbers | BN-3350 |
Product
Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutions, Inc., Knoxville, TN
Reason for recall
cGMP Deviation
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-579-2013. 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.