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. 2,578 recalls have been distributed to Utah in the last 12 months.
Showing 14261–14280 of 28,579 recalls
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Recalled by Compass Health Brands...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...
The Issue: A complaint trend was observed for post-operative loss of height and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...
The Issue: A complaint trend was observed for post-operative loss of height and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Potential loose cable connections on the reagent cooler, which could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...
The Issue: The manufacturer received complaints that customers were attempting to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test Recalled by...
The Issue: An elevated lot-to-lot bias was observed for Autoimmune EIA Anti-Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...
The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...
The Issue: Dental adaptor does not conform to specifications. The dental coupling of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...
The Issue: There is no warning in the Elekta Unity manual for the administration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.