Recalls affecting Kansas
Notices that name Kansas in their distribution area, plus every nationwide recall — nationwide recalls reach Kansas too.
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NHTSA safety recall · 11 months ago
Mercedes-Benz GLE 350 4MATIC recall: The center rear seat belts may have been installed without the child seat
The center rear seat belts may have been installed without the child seat protection function and fail to lock a child restraint properly. As such…
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NHTSA safety recall · 11 months ago
Mercedes-Benz AMG E 53 4Matic+ Wagon recall: The transmission wiring harness may be routed too close to the front
The transmission wiring harness may be routed too close to the front driveshaft, which can result in wiring harness damage and cause a loss of drive…
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NHTSA safety recall · 11 months ago
Ford Super Duty F-250 and F-350 recall: The right rear axle shaft may have been improperly heat-treated during
The right rear axle shaft may have been improperly heat-treated during manufacturing and may break.
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High - Class I · 11 months ago
Suzanna’s Kitchen Fully Cooked Breaded Chicken products recall: Misbranding; Unreported Allergens
Misbranding; Unreported Allergens
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NHTSA safety recall · 11 months ago
General GMC Canyon AT4X AEV recall: Incorrect sensing and diagnostic module (SDM) software may cause a second
Incorrect sensing and diagnostic module (SDM) software may cause a second stage passenger air bag deployment when only a first stage is intended. As…
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NHTSA safety recall · 11 months ago
BMW of X3 recall: While the vehicle is stationary, unexpected steering wheel movement
While the vehicle is stationary, unexpected steering wheel movement (rotation) may occur.
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Elevated risk · 11 months ago
Trek Electric Bicycles recall: Fall or Crash Hazard
Fall or Crash Hazard
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Class I · 11 months ago
ReBoost, ClearLife Nasal spray, 0.68 fl oz recall: Product has been found to contain yeast/mold and microbial contamination
Product has been found to contain yeast/mold and microbial contamination with one species identified as Achromobacter, at levels above specifications.
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NHTSA safety recall · 11 months ago
Volkswagen Tiguan recall: The passenger occupant detection system (PODS) may experience a fault
The passenger occupant detection system (PODS) may experience a fault in the wiring and deactivate the front passenger air bag when the seat is…
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Class II · 11 months ago
Get Tested International Ab Continuous Glucose Monitor recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Philips North America Llc IntelliVue MP70. Product Number: M8007A recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Get Tested International Ab Estrogen & Progesterone Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Gut Microbiome Test Medium recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Vaginal PH Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Environmental Pollutants Profile Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Sorbitol Intolerance Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab IBS Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Neurotransmitters XL recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX450. Product Number: 866062 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Get Tested International Ab Melatonin Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Women s Hormone Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Philips North America Llc IntelliVue Patient Monitor MX750. Product Number: 866471 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.
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Class II · 11 months ago
Get Tested International Ab Fecal Occult Blood Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.
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Class II · 11 months ago
Get Tested International Ab Epstein-Barr Virus Test recall: Distribution without premarket approval/clearance
Distribution without premarket approval/clearance.