PlainRecalls

Flawless Beauty LLC

18 recalls on record · Latest: Feb 14, 2018

Flawless Beauty LLC Recall Insight

Flawless Beauty LLC appears on 18 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.021% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 14, 2018, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 18 entries, severity tagging shows 0 critical, 18 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 18 of 18 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Drug (18). The date window on this page runs from May 21, 2014 to Feb 14, 2018.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Drug Moderate Feb 14, 2018

Ling Zhi capsules

FDA Drug Moderate Feb 14, 2018

TP Drug Laboratories Vitamin C ampules

FDA Drug Moderate Feb 14, 2018

Relumins Vitamin C Solvent ampules

FDA Drug Moderate Feb 14, 2018

Tationil Glutathione, 600 mg/ 4 mL, polvere e solvente per soluzione iniettabile, Teofarma, s.r.l.

FDA Drug Moderate Feb 14, 2018

Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials

FDA Drug Moderate Feb 14, 2018

Tatiomax Gluatathione Whitening kits, 1400mg vials, Made in Japan

FDA Drug Moderate Feb 14, 2018

Laennec INJ, Placenta extract (human), 2mL vials, Manufactured by: GCJBP Corp, Korea

FDA Drug Moderate Feb 14, 2018

Reiki Glutathione Whitening kits

FDA Drug Moderate Feb 14, 2018

Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche

FDA Drug Moderate Feb 14, 2018

TAD Glutathione Whitening Kits lyophilized powder for injection, 600 mg vials, 10 vials + 10 amps x 4 mL, Manufactured by: Biomedica Foscama Industri…

FDA Drug Moderate Feb 14, 2018

Saluta Glutathione Whitening kits, packaged in 600 mg, 1200 mg and 1800 mg glass vials, Manufactured by: Shandong Luye Pharmaceutical Co, Ltd, Yanta…

FDA Drug Moderate Feb 14, 2018

Sterilized water for injections BP, 50 x 5 mL plastic ampules, Manufactured in India

FDA Drug Moderate May 21, 2014

Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection vials, 1200 mg/200 mg, 10-count vials per box, Manufactured by: Sujie Pharmac…

FDA Drug Moderate May 21, 2014

Sterile Water for Injection, 5 mL ampoules, packaged in 50-count ampoules per box, Manufactured and Distributed by: Euro Med Laboratories, UPC 480057…

FDA Drug Moderate May 21, 2014

Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable solution, 1500 mg/500 mg, packaged in 8-count vials, 8-count 5 mL vitami…

FDA Drug Moderate May 21, 2014

Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution, 1 gm/0.35 gm, 5 mL ampoules, packaged in 10-count ampoules per box, Laboratorie…

FDA Drug Moderate May 21, 2014

Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed by: QAF Pharmaceuticals Inc. Ph…

FDA Drug Moderate May 21, 2014

Vitamin C (ascorbic acid) Injection, USP, 500 mg per 2 mL, 50 x 2 mL ampoules per box, Manufactured by: TP Drug Laboratories (1969) Co., Ltd., 98 Soi…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds