Relumins Advanced Glutathione kits recall
Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials
Why was Relumins Advanced Glutathione kits recalled?
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with Consent Decree of Permanent Injunction ordered by the United States District Court due to misbranding and unapproved new drugs pursuant to the FD&C Act.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
all lots
- Product
- Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials
- Recalling firm
- Flawless Beauty LLC
- Quantity
- N/A
- Distribution
- Product was distributed U.S.A. nationwide.
- Recall date
- February 14, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)