Ultra Seal Corporation 2022-02-09 Health serious FDA
Health · FDA · Recall #FDA-D-0467-2022
Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet… Recall
Issued February 9, 2022 · Ultra Seal Corporation
In February 2022, Ultra Seal Corporation recalled the Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
cGMP deviations
What you should do
- 1 Stop using Maximum Strength Non Aspirin Pain Reliever/Fever Reducer (acetaminophen 500 mg) 2 tablet… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Ultra Seal Corporation 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
- Ultra Seal Corporation
- Category
- Health
- Recall date
- February 9, 2022
- Units affected
- Not reported
- Sold at
- Nationwide within the United States
- Recall number
- FDA-D-0467-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Ultra Seal Corporation has 27 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.