Vehicles & car seats
Rossmonster Vans LLC: Printed Circuit Board May Overheat
An overheated printed circuit board increases the risk of a fire.
· NHTSA · 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, 2:53 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”
Vehicles & car seats
General Motors, LLC: Rearview Camera May Display Distorted or Blank Image
A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seatsKids & Babies
Britax Child Safety, Inc.: Child Seat Carrying Handle May Detach
A child may fall after a partial detachment, increasing the risk of injury.
· NHTSA · Nationwide
Medicines & devicesClass I
B BRAUN MEDICAL INC recalls 0
Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene
· FDA · Nationwide
Medicines & devicesClass III
Chiesi USA, Inc. recalls Revcovi (elapegademase-lvlr) Injection
Failed Stability Specifications: Out of specification stability result for the protein concentration profile.
· FDA · MO, TN
Medicines & devicesClass II
Cardinal Health 200, LLC recalls Presource Packs containing Medtronic Microstream Components: Intubation Kit Catalog Numbers AN23366084 AN23366
Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the patient's endotracheal tube to perform a pro
· FDA
Medicines & devicesClass II
Stryker Sustainability Solutions recalls 6 products
Reusable access port system may crack or seperate during use.
· FDA · Nationwide
Medicines & devicesClass II
NOXBOX LTD recalls NOxBOXi Nitric Oxide Delivery System
Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.
· FDA · Nationwide
Medicines & devicesClass I
BD SWITZERLAND SARL recalls BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set
Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance.
· FDA · 53 states
Vehicles & car seats
E-One Incorporated: Hydraulic Valve May Fail and Prevent Outrigger Operation
The inability to extend or retract the outriggers can delay emergency response, increasing the risk of injury.
· NHTSA · Nationwide
Vehicles & car seats
Avride Inc.: ADS Software May Cause Unexpected Vehicle Movement
Unexpected vehicle movement may increase the risk of a crash.
· NHTSA · Nationwide
FoodClass II
Dreyer's Grand Ice Cream Inc. recalls 6 products
Foreign object: products may contain glass pieces
· FDA · 34 states
Medicines & devicesClass II
Radiometer Medical ApS recalls The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists
In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood samples no longer suitable for testing FHbF and ctBil, 2) Re
· FDA · Nationwide
Medicines & devicesClass II
Cadwell Industries Inc recalls Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number: 190296-200 UDI-DI code: 0084006710
Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the patient, or allow an unintended electrical current to reach
· FDA · Nationwide
Medicines & devicesClass II
Stryker Sustainability Solutions recalls BARD EP XT DECAPOLAR STEERABLE
Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to particulate embolization, infection, thrombus or ganuloma formati
· FDA · Nationwide
Medicines & devicesClass II
Percussionaire Corporation recalls 7 products
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting
· FDA · Nationwide
Medicines & devicesClass II
Cardinal Health 200, LLC recalls 4 products
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user diss
· FDA · Nationwide
Medicines & devicesClass II
Wright Medical Technology, Inc. recalls CHARLOTTE CLAW Screw
Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads, which if used would prevent a secure rigid engagement with the pl
· FDA · Nationwide
FoodClass I
Indus Foods, LLC DBA Gangothri Foods Recalls Ready-To-Eat Pickled Goat and Chicken Products Produced Without Benefit of Inspection
High - Class I · Class I
· USDA FSIS · Nationwide
FoodClass I
Asian America Trading, Inc. Recalls Ineligible Siluriformes Fish Products Imported From the People’s Republic of China
High - Class I · Class I
· USDA FSIS · CA
FoodClass I
The Better Bakehouse Snack Company recalls Donutful Chocolate Dipped Vanilla Cake Donuts - 7
Undeclared Milk.
· FDA · Nationwide
FoodClass II
Best Friends Bakery, LLC recalls PUMPKIN SPICE NO BAKE COOKIE NET WT 3
Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
· FDA · 10 states
Medicines & devicesClass I
Baxter Healthcare Corporation recalls Dextrose Injection
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
· FDA · Nationwide
Medicines & devicesClass I
Baxter Healthcare Corporation recalls 0
Presence of particulate matter: Particulates identified as fiberglass
· FDA
Medicines & devicesClass II
Mylan Pharmaceuticals Inc recalls Prasugrel Tablets
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria
· FDA · Nationwide
Medicines & devicesClass II
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Revised C-Reactive Protein (RCRP)
The potential for falsely elevated results.
· FDA · Nationwide
Vehicles & car seats
Holley Performance Products: Loss of Throttle Control
A loss of throttle control increases the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
The Heil Co.: Ladder Bolt May Damage CNG Cylinders
A damaged CNG tank can leak fuel, increasing the risk of a fire.
· NHTSA · Nationwide
Vehicles & car seats
The Heil Co.: Ladder Bolt May Damage CNG Cylinders
A damaged CNG tank can leak fuel, increasing the risk of a fire.
· NHTSA · Nationwide
Vehicles & car seats
Ring Power Corporation: Cracked Weld May Cause Pole Guide Arm to Fall
Without a retaining pin, the pole guide arm may fall, increasing the risk of injury to people around the truck.
· NHTSA · Nationwide
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.