HIGH
CPSC
Great Lakes Wholesale International Recalled Great Lakes Select Battery Packs for Ingestion Risk (
Great Lakes Wholesale International
The button
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Vehicles & Parts
HIGH
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
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
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 DEVICE
Olympus Resection Inner 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
Olympus Inner Sheath Recalled Over Breaking Ceramic Tip 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 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 Recalled 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 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
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
Olympus Inner Sheath Recalled Due to Breakage Risk
Olympus Corporation of the Americas recalled the Inner Sheath 21 Fr., Model No. A2660T, on November 11, 2025. The recall follows reports of the ceramic tip breaking during use. Patients and healthcare providers should 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 Ceramic Tip
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 Inner 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
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 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
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
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
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