Published recall report · Quality failureUpdated · 6 yr 1 mo ago
Sanofi-Aventis U.S. LLC recall: Elitek (rasburicase) for injection, 7.5 mg vial, Rx Only Mfd. by Sanofi - Aventis U. S. LLC Bridgewater, NJ, 08807, NDC 0024-5151-75
Elitek (rasburicase) for injection, 7.5 mg vial, Rx Only Mfd. by Sanofi - Aventis U. S. LLC Bridgewater, NJ, 08807, NDC 0024-5151-75
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
Elitek (rasburicase) for injection, 7.5 mg vial, Rx Only Mfd. by Sanofi - Aventis U. S. LLC Bridgewater, NJ, 08807, NDC 0024-5151-75
- Producer
- Sanofi-Aventis U.S. LLC
- Brand
- ELITEK
A9306
- Dates on pack
- Lot #: A9306, Exp 2/28/2022
More detail
Failed Stability Specifications: Out of Specification result for enzyme activity levels noted during routine stability testing.
In the news
Reporting from news publishers. Follow the official notice for product advice.
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