Medicines & devicesClass I
Abiomed, Inc. recalls 3 products
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
· FDA · Nationwide
Recalls
Safety recalls that rarely make the news, straight from the official U.S. agency records (FDA, USDA, CPSC, NHTSA). Every listing links to its official notice. We only copy what the record says.
Checked Nov 3, 5:19 AM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
779 recalls for “AI”
Medicines & devicesClass II
Straumann USA LLC recalls GM Helix Implant
There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.
· FDA · Nationwide
Vehicles & car seats
Odyne Systems, LLC: High Voltage Battery May Fail and Cause Fire
Battery failure can also increase the risk of a fire.
· NHTSA · Nationwide
Vehicles & car seats
Mack Trucks, Inc.: Marker Lights May Fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
Volvo Trucks North America: Marker Lights May Fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
BMW of North America, LLC: Loss of Rear Wheel Power from Driveshaft Damage
An unexpected loss of drive power can increase the risk of a crash. In addition, a damaged driveshaft can result in a vehicle rollaway if the parking brake is not applied, increasing the risk of a crash or injury.
· NHTSA · Nationwide
Vehicles & car seats
BMW of North America, LLC: Incorrectly Attached Steering Spindle
An incorrectly attached steering spindle can lead to a loss of steering control, increasing the risk of a crash.
· NHTSA · Nationwide
FoodClass IIUpdated
Byron White Formulas, Inc. recalls 3 products
Label does not declare walnuts in English
· FDA · 50 states
Medicines & devicesClass II
Shanghai United Imaging Healthcare Co., Ltd. recalls 12 products
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from
· FDA · Nationwide
Medicines & devicesClass I
Medline Industries, LP recalls 7 products
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin
· FDA · Nationwide
Medicines & devicesClass II
Baxter Healthcare Corporation recalls 2 products
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
· FDA · Nationwide
FoodClass II
Africando Foods LLC recalls Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICANDO FOODS
Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
· FDA · IA, IL, KY
Medicines & devicesClass I
Fresenius Kabi USA, LLC recalls Tyenne (tocilizumab-aazg) Injection
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
· FDA · Nationwide
Medicines & devicesClass II
American Contract Systems Inc recalls 3 products
Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the manufacturing process. Use of a contaminated wipe may lead to lo
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls 2 products
Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls 5 products
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neu
· FDA · Nationwide
Medicines & devicesClass II
Cardinal Health 200, LLC recalls 2 products
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient harm or may lead to localized skin or s
· FDA · Nationwide
Medicines & devicesClass I
AVID Medical, Inc. recalls 4 products
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
· FDA · IL, NC, VA, WY
Medicines & devicesClass I
Bard Access Systems, Inc. recalls 2 products
this is a downstream recall of class I recall RES 98777
· FDA · 50 states
Medicines & devicesClass II
Fresenius Medical Care Renal Therapies Group, LLC recalls 4 products
Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovolemia.
· FDA · Nationwide
Vehicles & car seats
Daimler Trucks North America, LLC: Fuel Tank Cage Incompatible with Fuel System/FMVSS 301
During a crash, an incompatible fuel tank cage and fuel system may result in a fuel leak, increasing the risk of a fire.
· NHTSA · Nationwide
Vehicles & car seats
Daimler Trucks North America, LLC: Fuel Tank Cage Incompatible with Fuel System/FMVSS 301
During a crash, an incompatible fuel tank cage and fuel system may result in a fuel leak, increasing the risk of a fire.
· NHTSA · Nationwide
Vehicles & car seats
Marion Body Works Inc.: Touch Screen Display May Fail
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.
· NHTSA · Nationwide
Vehicles & car seats
Blue Bird Body Company: Damaged Wiring May Disrupt Critical Safety Functions
An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
Blue Bird Body Company: Damaged Wiring May Disrupt Critical Safety Functions
An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.
· NHTSA · Nationwide
FoodPublic Health Alert
FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been Recalled Due To Possible Salmonella Contamination
Public Health Alert · Public Health Alert
· USDA FSIS · Nationwide
FoodClass I
City Foods, Inc. Recalls Ready-To-Eat Pastrami and Corned Beef Products Due To Possible Listeria Contamination
High - Class I · Class I
· USDA FSIS · Nationwide
FoodClass IUpdated
Taylor Fresh Foods Inc recalls 25 products
Potential contamination with Salmonella.
· FDA · 27 states
FoodClass IUpdated
WFM Purchasing, LP recalls 10 products
Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.
· FDA · 13 states
FoodClass I
Shan Distribution Network, Inc. Recalls Ineligible Frozen Siluriformes Breaded Fish Fillet and Stick Products Imported from the United Arab Emirates
High - Class I · Class I
· USDA FSIS · IA, IL, IN, MI, MN, MO, OH, WI
Recall data comes from official U.S. government sources: openFDA (food, drugs, devices), USDA FSIS (meat, poultry, egg products), CPSC (consumer and children’s products) and NHTSA (vehicles, equipment, car seats). openFDA notes its data should not be relied on for medical decisions. Always confirm with the official notice. Check your vehicle by VIN at nhtsa.gov/recalls.