Recalls affecting Rhode Island
Notices that name Rhode Island in their distribution area, plus every nationwide recall — nationwide recalls reach Rhode Island too.
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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.
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Class II · 11 months ago
Get Tested International Ab Neurotransmitters Basic 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 MX550. Product Number: 866066 recall: Potential issue where the IntelliVue monitors did not alarm
Potential issue where the IntelliVue monitors did not alarm.