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. 2,627 recalls have been distributed to Utah in the last 12 months.
Showing 8701–8720 of 28,579 recalls
Recalled Item: ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray...
The Issue: Potential safety issue under specific preconditons that may result in a user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...
The Issue: The chrome surface of the push brace can crack during use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...
The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a software issue associated with the ability to properly complete a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...
The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw Recalled by Wright...
The Issue: Incorrect product is contained in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPELA FHD PTZ TILE KITS with Axis cameras used in Recalled by Natus...
The Issue: Tile kits that allow one to install and situate a video camera within a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michels Transport Medium Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.