immediate action Recalls

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 Convenience Kits Recalled Over Sterility Issues

Medline Recalls Neuro Shunt Kits Over Sterility Concerns

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 Lithotomy Packs 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.

FORD 2025 F-250 SD Recalled for Brake Pedal Pushrod May Disconnect

VANTIVE US HEALTHCARE Recalls Dialyzer Over Dislodgement Risk

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US Healthcare Recalls Dialyzer Over Dislodgement Risk

VANTIVE US Healthcare recalled 230,596 units of the PRIMSAFLEX M100 Set on January 6, 2026. The recall follows a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.

VANTIVE US HEALTHCARE Recalls Dialyzer Due to Dislodgement Hazard

VANTIVE US HEALTHCARE recalled 87,436 Prismaflex ST100 Dialyzers on January 6, 2026. The recall follows reports of potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.

VANTIVE US Healthcare Recalls Dialyzer Over Dislodgement Risk

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

VANTIVE US HEALTHCARE Recalls Dialyzer Due to Dislodgement Hazard

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

HerbsForever Recalls Ayurvedic Supplement Over Allergen Risk

Potential undeclared allergen ingredient (Wheat)

Herbs Forever Recalls Ayurvedic Supplement Due to Allergen Risk

Potential undeclared allergen ingredient (Wheat)