Ifosfamide Injection 1g/20mL — Class II drug recall D-1065-2013
Terminated recall by AmeriSource Bergen, reported 2013-10-09, distributed nationwide. Temperature abuse: Certain vials of Ifosfamide IV products were not refrigerated at certain Amerisource Bergen
| Recall number | D-1065-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AmeriSource Bergen, Chesterbrook, PA, United States |
| Recall initiated | 2013-09-13 |
| Classified | 2013-09-27 |
| Reported by FDA | 2013-10-09 |
| Terminated | 2014-10-01 |
| Distributed | Nationwide (US) |
| Quantity | 49 vials |
| Reason classes | temperature control |
| NDC | 00069-4495-22 |
| Lot numbers | 02/15, 7800932, 7800933 |
Product
Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4495-22
Reason for recall
Temperature abuse: Certain vials of Ifosfamide IV products were not refrigerated at certain Amerisource Bergen Drug Corp distribution centers.
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-1065-2013. 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.