Drug product
Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution 3mL vial, packaged in a) 30-count (NDC 0487-0201-03), b) 60-count (NDC 0487-0201-60), Rx only, MFG: Nephron Pharma
D-1021-2022
Product summary
- Event
- Event 89646
- Status
- Terminated
- Classification
- Class III
- Quantity
- 56 pouches
- Official record key
drug-enforcement:D-1021-2022
Official wording
Reason: cGMP deviations: Temperature abuse
Code information: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Distribution pattern: USA nationwide.
Derived failure modes
-
Manufacturing or process control
cGMP deviations