Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials
Reported: February 14, 2018 Initiated: January 19, 2018 #D-0324-2018
Product Description
Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials
Reason for Recall
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.
Details
- Recalling Firm
- Flawless Beauty LLC
- Units Affected
- N/A
- Distribution
- Product was distributed U.S.A. nationwide.
- Location
- Asbury Park, NJ
Frequently Asked Questions
What product was recalled? ▼
Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials. Recalled by Flawless Beauty LLC. Units affected: N/A.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 14, 2018. Severity: Moderate. Recall number: D-0324-2018.
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