Health & Personal Care
HIGH
FDA DRUG
Elixir by Coco March Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations
SUNSCREEN
CGMP Deviations
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,434
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- 170
Health & Personal Care
HIGH
FDA DRUG
Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations (Class II)
Sugared+Bronzed
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
CA Botana Mineral Sunscreen Recall Covers 1,167 Tubes Over CGMP Deviations (2025)
MINERAL SUNSCREEN
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
CLEARSTEM You Are Sunshine SPF 50 Sunscreen Recalled for CGMP Deviations (Visage)
CLEARSTEM
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Weh-Weh Pain Reliever Gel Recalled for CGMP Deviations, 810 Tubes Affected (2025)
WEH-WEH PAIN RELIEVER GEL
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Ultra Umbrella Sunscreen by CA BOTANA Recalled for CGMP Deviations in 874 Tubes (HIGH Hazard)
CA BOTANA
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Lannett NIACIN ER 1,000 mg Recall Affects 46,848 Bottles Nationwide (2025)
Lannett
Failed Dissolution
Health & Personal Care
HIGH
FDA DRUG
Elixir by Coco March Mineral Sunscreen SPF 50 Recalled for CGMP Deviations, HIGH Hazard (2025)
Elixir
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Gabriel Mineral Sunscreen SPF 50 Recalled for CGMP Deviations in 1617 Tubes
Gabriel Mineral Sunscreen
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
470 Doctor D. Schwab Controlling Cream Tubes Recalled for CGMP Deviations
Doctor D. Schwab
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
555 Doctor D. Schwab Controlling Balm Tubes Recalled Over CGMP Violations
Doctor D. Schwab recalled 555 tubes of Controlling Balm with Tea Tree Oil after identifying CGMP deviations. The product may not meet quality standards, posing a safety risk. Consumers should stop using the balm immediately and contact CA BOTANA for guidance.
Doctor D. Schwab
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
CA Botana Doctor D. Schwab Shimmery Sun Lotion Sunscreen Recall for CGMP Deviations (2025)
Doctor D. Schwab
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Mylan Haloperidol Lactate Injection Recalled Over Labeling Errors
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
HALOPERIDOL LACTATE
Labeling: Not
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma FentaNYL Citrate PF IV Injection Recall 2025 Over Labeling Errors
STAQ Pharma recalled FentaNYL Citrate PF IV injection nationwide after labeling left incorrect or missing lot and expiration dates. Healthcare providers must stop using the product immediately. STAQ Pharma will provide recall instructions by letter.
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
ibspot Taoscare Motion Sickness Patches Recalled Over NDA/ANDA Issue (2025)
Marketed Without an Approved NDA/ANDA
ibspot
Marketed Without
Food & Beverages
HIGH
FDA FOOD
Rong Shing NY Recalls Aojia Dried Red Bayberry 5.6oz for Undeclared Sulfites (2025)
Product contains undeclared sulfites (7.39mg/serving) and cyclamates
Rong Shing Trading NY
Product contains
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Ketamine Hydrochloride Injection 50 mL Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Hydromorphone HCl PF 10mg/50mL IV Injection Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
USV Private Olopatadine Eye Drops 0.1% Recalled in 8,952 Bottles (2025)
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
USV Private
Failed Impurities/Degradation