ULTRAtab Laboratories, Inc. 2022-02-16 Health serious FDA
Health · FDA · Recall #FDA-D-0553-2022
Coated Back Relief Tablet (Acetaminophen 250 mg, Magnesium Salicylate 290 mg, Caffeine 50… Recall
Issued February 16, 2022 · ULTRAtab Laboratories, Inc.
In February 2022, ULTRAtab Laboratories, Inc. recalled the Coated Back Relief Tablet (Acetaminophen 250 mg, Magnesium Salicylate 290 mg, Caffeine 50…, 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 Coated Back Relief Tablet (Acetaminophen 250 mg, Magnesium Salicylate 290 mg, Caffeine 50… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact ULTRAtab Laboratories, 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
- ULTRAtab Laboratories, Inc.
- Category
- Health
- Recall date
- February 16, 2022
- Units affected
- Not reported
- Sold at
- Bulk product was distributed to 3 distributors who may have distributed finished product.
- Recall number
- FDA-D-0553-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- ULTRAtab Laboratories, Inc. has 18 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.