Published recall report · Quality failureUpdated · 1 yr 2 mo ago
Mckesson Medical-Surgical Inc. Corporate Office recall: PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21
PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21
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
PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21
- Producer
- Mckesson Medical-Surgical Inc. Corporate Office
- Brand
- PROLIA
1180924
- Dates on pack
- Lot: 1180924, Expiration date: 6/30/2027.
More detail
CGMP Deviations; potential temperature excursions due to transit delays
In the news
Reporting from news publishers. Follow the official notice for product advice.
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