Flawless Beauty LLC

Complete recall history across all FDA and CPSC categories — 18 total recalls

Flawless Beauty LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (18)

FDA drug safety enforcement actions by Flawless Beauty LLC

Date Product Reason Class
Jan 19, 2018 Sterilized water for injections BP, 50 x 5 mL plastic ampules, Manufactured i... Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Saluta Glutathione Whitening kits, packaged in 600 mg, 1200 mg and 1800 mg g... Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 TAD Glutathione Whitening Kits lyophilized powder for injection, 600 mg vials... Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Reiki Glutathione Whitening kits Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Laennec INJ, Placenta extract (human), 2mL vials, Manufactured by: GCJBP Corp... Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg v... Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Tationil Glutathione, 600 mg/ 4 mL, polvere e solvente per soluzione iniettab... Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Relumins Vitamin C Solvent ampules Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 TP Drug Laboratories Vitamin C ampules Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Jan 19, 2018 Ling Zhi capsules Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily re... Class II
Apr 29, 2014 Vitamin C (ascorbic acid) Injection, USP, 500 mg per 2 mL, 50 x 2 mL ampoules... Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the co... Class II
Apr 29, 2014 Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 1... Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use ... Class II
Apr 29, 2014 Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution, 1 gm/0.... Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose... Class II
Apr 29, 2014 Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable ... Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose... Class II
Apr 29, 2014 Sterile Water for Injection, 5 mL ampoules, packaged in 50-count ampoules per... Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose... Class II
Apr 29, 2014 Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection vials... Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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