Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,139 recalls have been distributed to Utah in the last 12 months.
Showing 641–660 of 28,579 recalls
Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX800. Product Number: 865240. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP30. Product Number: M8002A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP90. Product Number: M8010A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker MV3 bariatric bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Arise 1000EX mattress Recalled by Stryker Medical Division of...
The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP5. Product Number: M8105A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP20. Product Number: M8001A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO BrainPath Recalled by Stryker Corporation Due to Tape used to secure...
The Issue: Tape used to secure components within packaging contains latex, despite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OER-Elite Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MP80. Product Number: M8008A. Recalled by Philips North America...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...
The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Recalled by Medicrea International Due to Due to complaints,...
The Issue: Due to complaints, orthopedic rotation tool handle may untread from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips North America Llc Due to If the screws of...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...
The Issue: If the screws of tube heat exchanger on the rotating scanner are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...
The Issue: Treatment reagent functionality in respiratory specimens fluidification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1ml of DTT in liquid phase Recalled by Copan Italia Due to Treatment reagent...
The Issue: Treatment reagent functionality in respiratory specimens liquification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.