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. 2,471 recalls have been distributed to Utah in the last 12 months.
Showing 23981–24000 of 28,579 recalls
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Luminos dRF Recalled by Siemens Medical Solutions USA, Inc Due to It...
The Issue: It was discovered that during a RAD examination using Siemens Luminos dRF,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In line Valve with Unitized BACTISEAL¿ Catheter and...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Recalled by Codman &...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve only with SIPHONGUARD¿ Device Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...
The Issue: In specific situation a partially truncated file may be written to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Catheter and Accessories Recalled by...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas - In Line Valve with Unitized Catheter and Accessories...
The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....
The Issue: There was an error in manufacturing which resulted in the proximal lag screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...
The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.