stop use immediately Recalls

Cook Medical Recalls Transjugular Liver Access Set Over Hazardous Manufacturing

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Cook Medical Recalls Introducer Sheaths Over Manufacturing Errors

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Abbott Recalls FreeStyle Libre 3 Plus Sensors Due to Hazardous Readings

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 Recalls Custom Pak Surgical Packs Over Sterility Issues

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.

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

Draeger Vapor 2000 Anesthetic Vaporizer Recalled Over Impurities

A certain component of affected devices was not delivered within specification and contained impurities.

Draeger Vapor 3000 Anesthetic Vaporizer Recalled Due to Impurities

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.

Breckenridge Recalls Duloxetine Capsules Over Chemical Hazard

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

Abbott Recalls FreeStyle Libre 3 Plus Sensors Over Low Glucose Risk

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Abbott Recalls FreeStyle Libre 3 Plus Sensor Over Glucose Errors

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Changchun Wancheng Recalls Ovulation Test Over False Results Risk

Dr. Anna Cabeca Test Strips Recalled Over False Diagnostic Risks

Changchun Wancheng Recalls Male Fertility Test Over False Results

Changchun Wancheng Bio-Electron Co. recalled 1,000 male fertility sperm tests on November 22, 2025. The tests were distributed without proper FDA clearance and may yield inaccurate results. This could lead to inappropriate medical interventions by users.

Vivoo Vaginal pH Test Recalled Over Inaccurate Results Risk

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.

Changchun Wancheng Bio-Electron Recalls Vivoo pH Test for Inaccurate Results

Changchun Wancheng Bio-Electron Recalls Menopause Test Cassette

Fresenius Kabi Recalls Ivenix Infusion System Software Over Safety Issues

Fresenius Kabi USA recalled 30 units of the Ivenix Infusion System LVP Software on November 21, 2025. The recall addresses concerns related to programming instructions for LVP duration. Patients and healthcare providers must stop using the device immediately.

SB FOOD Recalls Gummy Candy Over Unallowed Color Additive

SB FOOD recalled 100 cases of Yoyo Gummy Assorted Flavor on November 21, 2025. The product contains an unapproved color, Carmoisine (E122), posing health risks. Consumers should not consume the candy and seek refunds.

Roche Diagnostics Recalling Anti-TSHR Immunoassay Over Diagnosis Risk

Roche Diagnostics Operations recalled 1,300 Anti-TSHR immunoassay cassettes on November 21, 2025. Variability in results may lead to incorrect diagnoses and treatment delays. The recall affects multiple states across the U.S.

Boar's Head Grated Cheese Recalled Due to Listeria Risk

Boar's Head recalled 405 bags of Pecorino Romano Grated cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a serious health risk. Consumers should not consume the cheese and seek a refund or replacement immediately.