FDA recalls Je Dois Lavoir's 365 SKINNY High Intensity Capsules due to undeclared sibutramine, a withdrawn drug with safety concerns. Consumers should stop using affected lots.
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NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.
Je Dois Lavoir is recalling 365 SKINNY High Intensity Capsules (600 mg, 30-count) because they contain undeclared sibutramine, a drug previously approved but withdrawn from the US market due to safety issues. This poses a risk of serious health effects if taken.
The capsules contain undeclared sibutramine, a drug that was approved in the US but later withdrawn because it caused serious health risks. This means the product could lead to adverse effects like heart problems or other serious health issues if taken.
Anyone who owns or uses the recalled 365 SKINNY High Intensity Capsules (600 mg, 30-count) from Je Dois Lavoir. People taking these capsules for weight loss are most at risk due to the undeclared sibutramine.
Check for the product name '365 SKINNY High Intensity Capsules', 600 mg, 30-count bottle, and the lot number 102-26 (expired December 2022).
Immediately stop taking the recalled capsules as they contain undeclared sibutramine, a drug withdrawn from the US market due to safety concerns.
FDA analysis found the product contains undeclared sibutramine, a drug previously approved but withdrawn from the US market due to safety concerns.
Stop using the capsules immediately. The product is recalled due to the presence of undeclared sibutramine, which poses serious health risks.
The recall record does not mention any replacement or refund options.
We’ve drafted a message you can send Je Dois Lavoir to request your refund or repair — edit it as you like.
Subject: Recall D-0631-2022 — Je Dois Lavoir Je Dois Lavoir Hello, I own a Je Dois Lavoir that is covered by recall D-0631-2022 from Je Dois Lavoir. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
