Vehicles & car seats
Forest River Bus, LLC: Wheelchair Lift May Inadvertently Move
A wheelchair lift that continues to move while occupied increases the risk of injury.
· NHTSA · Nationwide
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 2, 11:30 PM 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.
1105 recalls
Vehicles & car seats
A wheelchair lift that continues to move while occupied increases the risk of injury.
· NHTSA · Nationwide
Vehicles & car seats
A detach light tower can become a road hazard for other vehicles, increasing the risk of a crash or injury.
· NHTSA · Nationwide
Vehicles & car seats
Unvented exhaust fumes increase the risk of injury from carbon monoxide poisoning.
· NHTSA · Nationwide
Vehicles & car seats
Rear coil springs that detach from the vehicle while driving increase the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
A loss of electronic stability control increases the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
A TPMS warning light that fails to notify the driver of low tire pressure increases the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
A lateral link separation could shift the wheel alignment, causing a loss of vehicle control and increasing the risk of a crash.
· NHTSA · Nationwide
Medicines & devicesClass II
Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
· FDA · 52 states
Medicines & devicesClass II
Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.
· FDA · Nationwide
Medicines & devicesClass II
Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH).
· FDA · Nationwide
Medicines & devicesClass III
Failed dissolution specifications.
· FDA · Nationwide
Medicines & devicesClass II
Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.
· FDA · Nationwide
Medicines & devicesClass II
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam sterilization cycles, the potential hazard is that the biological indicator
· FDA · Nationwide
Medicines & devicesClass III
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm functions
· FDA · Nationwide
Vehicles & car seats
LP tanks that cannot be shut off increase the risk of a fire. Additionally a loose LP tank may detach and become a road hazard, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
A wheelchair lift that continues to move while occupied increases the risk of injury.
· NHTSA · Nationwide
Vehicles & car seats
The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
Incorrect information may result in the wrong sized replacement tires being installed, increasing the risk of a crash.
· NHTSA · Nationwide
FoodClass II
Product contains garlic essential oil not approved for culinary use
· FDA · 13 states
FoodClass III
Unapproved dye Ponceau 4R
· FDA · 15 states
FoodClass I
Potential E. coli O145:H28 Contamination
· FDA · AR
Medicines & devicesClass II
Defective Delivery System: Possibility of no medication in the prefilled pen.
· FDA · Nationwide
Medicines & devicesClass II
A navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch MacBook Pro battery, subject to an Apple battery recall, that may overheat
· FDA · Nationwide
Medicines & devicesClass II
Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.
· FDA · Nationwide
Medicines & devicesClass II
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction w
· FDA · Nationwide
Vehicles & car seats
A detached winch may increase the risk of injury to people near the trailer.
· NHTSA · Nationwide
Vehicles & car seats
Referencing the incorrect weight could result in the trailer being overloaded, increasing the risk of a crash.
· NHTSA · Nationwide
Medicines & devicesClass III
Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification.
· FDA · Nationwide
Medicines & devicesClass II
The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.
· FDA · AZ, CA, FL, IN, LA, NV, RI
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.