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
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
3,598 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 3,598
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
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
HIGH
HIGH
CPSC
ESR HaloLock Wireless Power Banks Recalled in Expansion to Include 2G505 Model for Fire and Burn Haz
ESR HaloLock
The lithium-ion
HIGH
CPSC
Bellabu Bear Recalls Bamboo Sherpa Children's Robes for Burn Hazard (2025)
Bellabu Bear
The recalled
HIGH
Health & Personal Care
HIGH
FDA DRUG
Sucralfate Tablets Recalled by American Health Packaging for CGMP Deviations (27,868 Packs, 2025)
Sucralfate
CGMP Deviations:
HIGH
CPSC
Calico Brands Recalls Scripto Premium Torch for Fire and Burn Hazard (2025)
Calico Brands
The recalled
HIGH
HIGH
HIGH
CPSC
Tempo USA Recall: Ambiano Electric Pressure Cookers Recalled Over Serious Burn Hazard (2025)
Tempo USA
The pressure-cooker
HIGH
CPSC
Generic Magnetic Ball Sets Recalled for Magnet Ingestion Risk Sold on Amazon by Ritons (2025 recall)
Generic Magnetic Ball Sets
The recalled
HIGH
CPSC
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.
Living Glow
The lithium-ion
Health & Personal Care
HIGH
FDA DEVICE
Glycar SA Recalls 18 SJM Pericardial Patch EnCap 5x10 cm REF C0510 in 2025 Recall
The impacted lot may not meet the required tensile strength specification.
Glycar SA
The impacted