Abbott Diabetes Care Recalls FreeStyle Libre 3 Sensor Over Glucose Reading Errors
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Recall database
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Alcon Laboratories, Inc. recalled 151 units of Custom Pak surgical procedure packs on November 24, 2025. The recall stems from incomplete seals that may affect sterility. Healthcare providers and patients should stop using the products immediately.
Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.
A certain component of affected devices was not delivered within specification and contained impurities.
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.
Potential presence of Listeria monocytogenes.
GBC Food Services recalled 11 units of EverRoast Chicken Caesar Wrap on November 22, 2025. The recall occurred due to potential contamination with Listeria monocytogenes. The affected products were distributed in Kentucky and Indiana.
Changchun Wancheng Bio-Electron Co. recalled 1,000 units of S. Typhi/Para Typhi A Antigen test strips on November 22, 2025. The recall affects tests distributed nationwide, which may produce false results and lead to inappropriate medical intervention.
Vivoo recalled 3,000 vaginal pH tests on November 22, 2025. The tests may cause false results leading to inappropriate medical interventions. The products were distributed nationwide, including Texas, Georgia, and California.