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
- High-risk recalls
- 4,267
- 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
Medline Convenience Kits Recalled Due to Sterilization Issues
Medline Convenience Kits Recalled Due to Sterility Issues
Medline Recalls Surgical Kits Due to Sterility Assurance Issues
Medline Surgical Kits Recalled Over Sterilization Issues
Medline Industries recalled 4,415 surgical kits on January 7, 2026, due to sterilization calibration issues. These issues could compromise the sterility assurance level of the products. Healthcare providers and patients must stop using the kits immediately.
Medline Surgical Packs Recalled Over Sterility Concerns
Medline Industries recalled 193,157 surgical packs on January 7, 2026, due to sterility assurance issues. The recall affects two model numbers: DYNJP1050UG and DYNJP8401. Healthcare providers and patients must stop using these products immediately.
Medline Recalls Burn Care Kits Due to Sterility Issues
Medline Industries recalled 291 units of burn care kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Users should stop using the affected products immediately.
Medline Recalls Tracheostomy Kits Over Sterility Concerns
Medline Recalls Admission Kits Over Sterility Concerns
Medline Industries recalled 1,070 ADMIT KITS due to calibration issues affecting sterilization. The recall, effective January 7, 2026, has been classified as Class II. Healthcare providers must stop using these kits immediately to ensure patient safety.
Medline Recalls Convenience Kits Over Sterility Concerns
Medline recalled 553 units of its Convenience Kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Healthcare providers and patients must stop using the affected devices immediately.
Ford Recalls 2020-2025 Explorer and Aviator for Second-Row Seat Switch Bezel Issue (25S67)
Ford Motor Company (Ford) is recalling certain 2020-2025 Aviator, and Explorer vehicles. The switch for the easy-entry second-row outer seats may bind or stick, resulting in the seats unlatching, folding, or sliding unexpectedly while driving.
Ford 2025 Explorer Recall for Engine Long-Block Defects
Ford Motor Company (Ford) is recalling certain 2025 Transit, F-150, and Explorer vehicles. The connecting rod and rod bearing components may have manufacturing defects that can lead to engine damage and engine failure.