AptaPharma Inc. 2022-05-04 Health moderate FDA
Health · FDA · Recall #FDA-D-0787-2022
Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed… Recall
Issued May 4, 2022 · AptaPharma Inc.
In May 2022, AptaPharma Inc. recalled the Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed…, a moderate health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Incorrect/Undeclared Excipient: Product contains alcohol
What you should do
- 1 Stop using Wal-Tussin DM (dextromethorphan HBr/Guaifenesin), 12 FL OZ (354 mL) bottles, Distributed… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact AptaPharma Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- AptaPharma Inc.
- Category
- Health
- Recall date
- May 4, 2022
- Units affected
- Not reported
- Sold at
- IL only
- Recall number
- FDA-D-0787-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- AptaPharma Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.