stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
CA Botana Doctor D. Schwab Shimmery Sun Lotion Sunscreen Recall for CGMP Deviations (2025)
Dr. Bump Gel Menthol 5% Recall for 4,890 Bottles Over CGMP Deviations
Major Pharmaceuticals Gabapentin 100 mg 10-Capsule Recall Nationwide 2025
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
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.
470 Doctor D. Schwab Controlling Cream Tubes Recalled for CGMP Deviations
Gabriel Mineral Sunscreen SPF 50 Recalled for CGMP Deviations in 1617 Tubes
Elixir by Coco March Mineral Sunscreen SPF 50 Recalled for CGMP Deviations, HIGH Hazard (2025)
Lannett NIACIN ER 1,000 mg Recall Affects 46,848 Bottles Nationwide (2025)


Bellabu Bear Recalls Bamboo Sherpa Children's Robes for Burn Hazard (2025)
Rong Shing NY Recalls Aojia Dried Red Bayberry 5.6oz for Undeclared Sulfites (2025)
Product contains undeclared sulfites (7.39mg/serving) and cyclamates

Generic Magnetic Ball Sets Recalled for Magnet Ingestion Risk Sold on Amazon by Ritons (2025 recall)

Living Glow Portable Waist Fans Recalled for Fire Hazard, High Risk Lithium-Ion Battery
Living Glow recalled for a fire hazard. Guangzhou Jiguang Lighting manufactured the waist fan sold by HSN from May 2025 through July 2025 for $20-$25. Consumers should immediately stop using the recalled device and register for a full refund.

ibspot Taoscare Motion Sickness Patches Recalled Over NDA/ANDA Issue (2025)
Marketed Without an Approved NDA/ANDA


Calico Brands Recalls Scripto Premium Torch for Fire and Burn Hazard (2025)
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.
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.