Je Dois Lavoir LLC 2022-02-23 Health critical FDA
Health · FDA · Recall #FDA-D-0631-2022
365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL Recall
Issued February 23, 2022 · Je Dois Lavoir LLC
In February 2022, Je Dois Lavoir LLC recalled the 365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL, a critical 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
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.
What you should do
- 1 Stop using 365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Je Dois Lavoir LLC 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
- Je Dois Lavoir LLC
- Category
- Health
- Recall date
- February 23, 2022
- Units affected
- Not reported
- Sold at
- Sold online via website nationwide in the USA and Canada.
- Recall number
- FDA-D-0631-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Je Dois Lavoir LLC has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.