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. 2,666 recalls have been distributed to Utah in the last 12 months.
Showing 3281–3300 of 28,579 recalls
Recalled Item: AGILE ESO FC RMV 23MM X 10.1CM IN 18.5 F-Agile Recalled by Boston Scientific...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marodyne-LiV Recalled by Btt Health Gmbh Due to Some power supply units in...
The Issue: Some power supply units in Austria and Germany had a voltage drop in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Primary Administration Set Recalled by Fresenius Kabi USA, LLC Due to A...
The Issue: A defect may cause an uncontrolled medication flow condition which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 4340 Respiratory Sensing Lead Recalled by Inspire Medical...
The Issue: Labeling error with a mismatch between the shelf box serial number label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 4063 Stimulation Lead Recalled by Inspire Medical Systems Inc....
The Issue: Labeling error with a mismatch between the shelf box serial number label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 620G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed Insulin Pump Device. MiniMed 670G Recalled by Medtronic MiniMed,...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stainless Steel Sims Uterine Sound Recalled by CooperSurgical, Inc. Due to...
The Issue: During the manufacturing process the devices were laser-marked with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silver-Plated Copper Sims Uterine Sound Recalled by CooperSurgical, Inc. Due...
The Issue: During the manufacturing process the devices were laser-marked with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...
The Issue: During manufacturing, the last three tests from the 160 test flex of lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...
The Issue: Potential for the front lever chain of the DR 800 table to fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Recalled by...
The Issue: Reports have been received regarding open seals on the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiomarC EX Fiducial Marker System Recalled by Carbon Medical Technologies,...
The Issue: This recall has been initiated due to a failure to provide an MRI Insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (250 Test - REF)-In vitro diagnostic Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 (250 Test)-In vitro diagnostic use in Recalled by...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.