ULTRAtab Laboratories, Inc. 2022-02-16 Food serious FDA
Food · FDA · Recall #FDA-F-0729-2022
MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY Recall
Issued February 16, 2022 · ULTRAtab Laboratories, Inc.
In February 2022, ULTRAtab Laboratories, Inc. recalled the MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY, a serious food 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 MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY 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
- Food
- Recall date
- February 16, 2022
- Units affected
- Not reported
- Sold at
- Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
- Recall number
- FDA-F-0729-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- ULTRAtab Laboratories, Inc. has 18 recalls in our database.
- We're tracking 3,082 Food recalls in our database.
- This is the 671st Food recall we've logged in 2022.