Visalia, CA, United States
Je Dois Lavoir LLC recalls
1 recall recorded since 2018, most recently on 2 August 2021. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)1
Terminated Class I Drugs
- Recall started
- 2 August 2021
- Terminated
- 2 May 2023
- Reason
- 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NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.
- Distribution
- Sold online via website nationwide in the USA and Canada.
- Initiated
- Voluntary: Firm initiated
- Recall number
- D-0631-2022
- 365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.