HIGH
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DRUG
Lupin Pharmaceuticals Recalls Ganirelix Acetate Injection for Impurity Risk
Lupin Pharmaceuticals recalled 32,736 vials of Ganirelix Acetate Injection on November 13, 2025. The recall follows the discovery of impurities in the drug. Consumers and healthcare providers should stop using the product immediately to avoid health risks.
GANIRELIX ACETATE
Failed impurities/degradation
Food & Beverages
HIGH
FDA FOOD
Santos Agency Recalls Brass Langri Cookware Over Lead Risk
Santos Agency recalled Brass Langri Cookware on November 12, 2025, due to potential lead contamination. Consumers should not use the product and seek a refund. The affected item features sticker label: 14.
Santos Agency
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
Stryker Recalls CranialMask Tracker Due to Device Error
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.
Howmedica Osteonics
When the
Food & Beverages
HIGH
FDA FOOD
Stuffed Foods Recalls Cacio e Pepe Arancini Over Soy Allergy Risk
Stuffed Foods
Undeclared Soy
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health Recalls ChemoPlus Gowns Over Expiration Date Error
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
Cardinal Health 200
Affected gowns
Food & Beverages
HIGH
FDA FOOD
Genepro Protein Recalls 250-Bag Whey 4th Gen Plasma-Treated Protein for Milk Allergen Labeling Error
Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen
Genepro Protein
Product is
Health & Personal Care
HIGH
FDA DRUG
Walgreens Saline Nasal Spray With Xylitol Recalled for Microbial Contamination (41,328 Bottles, 2025
Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
Medical Products Laboratories
Microbial contamination
Vehicles & Parts
HIGH
Health & Personal Care
HIGH
FDA DEVICE
AVID Medical Recalls Halyard MINI PLUS KIT SOUTH Over Transplant Risk
AVID Medical recalled 380 units of the Halyard MINI PLUS KIT SOUTH on November 11, 2025. The devices are unsuitable for organ transplant procedures, posing potential health risks. Healthcare providers and patients must stop using the device immediately.
AVID Medical
Devices are
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breaking Tip Hazard
Olympus Corporation of the Americas recalled 2,626 units of its Resection Sheath on November 11, 2025. The ceramic tip of the sheath may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breaking Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Ceramic Tip Breaking
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Ceramic Tip Breakage
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Endoscopic Sheath Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breakage Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breaking Tips
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
AVID Medical Recalls Organ Recovery Kit Due to Unsuitability
Devices are not suitable for organ transplant.
AVID Medical
Devices are
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of