HIGH
CPSC
Sunnyyes LED Mini Lights Recalled for Battery Ingestion Risk, Despite Reese’s Law Violations
Sunnyyes LED Mini Lights
The recalled
electrical hazard Recalls
1,120 recalls tagged with “electrical hazard”.
Health & Personal Care
HIGH
FDA DRUG
ARTIFICIAL TEARS Eye Drops Recalled for Sterility Concerns, 720 Bottles Distributed Nationwide (2026
Lack of Assurance of Sterility
ARTIFICIAL TEARS
Lack of
Health & Personal Care
HIGH
FDA DRUG
GE Healthcare Omnipaque Iohexol Injection Recall Expanded for Particulate Matter in 306,810 Vials (D
OMNIPAQUE
Presence of
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Vancomycin HCI Recall: 34,260 Bags with Break-Off-Part Risk (2026)
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron Compounding Services
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Vancomycin HCl 1 g in 250 mL NS Injection Recall Expands in 2026
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron Compounding Services
Lack of
HIGH
CPSC
Electrolux Group Recalls Frigidaire Gas Ranges for Burn Hazard (2026)
Electrolux Consumer Products, Inc., of Charlotte, North Carolina
The ovens
Health & Personal Care
HIGH
FDA DRUG
Curosurf 240 mg Poractant Alfa Recalled for Sterility Concerns (2026)
Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.
CUROSURF
Lack of
Health & Personal Care
HIGH
FDA DRUG
Xanax XR Alprazolam Recall Over Failed Dissolution Specifications Affects US Nationwide Distribution
XANAX
Failed Dissolution
Food & Beverages
HIGH
FDA FOOD
Pure Vitamins and Natural Supplements Blue Bull Extreme Recall for undeclared sildenafil (High risk)
FDA analysis revealed the presence of undeclared sildenafil
Pure Vitamins and Natural Supplements
FDA analysis
Food & Beverages
HIGH
FDA FOOD
Pure Vitamins and Natural Supplements Boner Bears Honey Recall for Undeclared Sildenafil and Tadalaf
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
Pure Vitamins and Natural Supplements
FDA analysis
Health & Personal Care
HIGH
FDA DEVICE
Brahms PlGF Plus KRYPTOR 859075N Recall Expands to 5,254 Units Worldwide (2026)
Brahms GmbH
Customers have
Health & Personal Care
HIGH
FDA DEVICE
Stryker Sustainability Solutions Color Cuff Recall Expands to 56,740 Cuffs Over Detachment Risk (202
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.
Stryker Sustainability Solutions
Due to
Vehicles & Parts
HIGH
NHTSA
Honda Recalls 2023-2025 Pilot and 2023-2024 Passport Over Fuel Tank Filler Leakage (2026)
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Passport and 2023-2025 Pilot vehicles. The fuel filler neck tube and fuel filler pipe may separate, allowing fuel to leak.
Honda
A fuel
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recall for Sterility Concerns (2026) Affecting US Nationwide, R
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi 1,000 mL Sodium Chloride Injection Recall for Sterility Concerns (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi Saline Solution Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
BD and Fresenius Kabi Sodium Chloride Injection Recalled for Lack of Sterility Assurance (2026)
Lack of Assurance of Sterility
SODIUM CHLORIDE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fresenius Kabi 5% Dextrose Injection Recall Active Over Sterility Assurance Issue (2026)
Lack of Assurance of Sterility
DEXTROSE
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Siemens ARTIS pheno and ARTIS Icono Imaging Systems Recalled for Dose-Display Anomaly (2026)
Siemens Medical Solutions USA
During patient
Health & Personal Care
HIGH
FDA DEVICE
Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled Over Expired-Lot
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook
Products from
Tag Statistics
Total Recalls
1,120