AptaPharma Inc.: Drug Recall
Recall #D-0787-2022 · 03/29/2022
Class III: Low Risk
Recall Details
- Recall Number
- D-0787-2022
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- AptaPharma Inc.
- Status
- Terminated
- Date Initiated
- 03/29/2022
- Location
- Pennsauken, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 40000 - 50000 units
Reason for Recall
Incorrect/Undeclared Excipient: Product contains alcohol
Product Description
Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0324-28.
Distribution Pattern
IL only
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.