CARDINAL HEALTHCARE: Drug Recall
Recall #D-0163-2024 · 01/26/2022
Class II: Risk
Recall Details
- Recall Number
- D-0163-2024
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- CARDINAL HEALTHCARE
- Status
- Terminated
- Date Initiated
- 01/26/2022
- Location
- Dublin, OH, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 11 cartons
Reason for Recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Product Description
ALBUTEROL SULFATE IN 90MCG per actuation, 200 Metered Inhalations, Rx Only, 8.5 g Net Contents, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India. NDC: 68180-963-01
Distribution Pattern
Nationwide USA
Other Recalls by CARDINAL HEALTHCARE
- Class II: Risk 01/26/2022
- Class II: Risk 01/26/2022
- Class II: Risk 01/26/2022
- Class II: Risk 01/26/2022
- Class II: Risk 01/26/2022
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.