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. 2,650 recalls have been distributed to Utah in the last 12 months.
Showing 4141–4160 of 28,579 recalls
Recalled Item: CROME HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to Potential...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT HF CDT-D MRI SureScan Recalled by Medtronic Inc. Due to Potential...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA MRI S DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMO MRI VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT XT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRRO MRI DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA MRI S DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Blueprint Software Recalled by Tornier S.A.S. Due to The software...
The Issue: The software bug allows for case planning with anatomic glenoid Perform /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyoSPECT System Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING...
The Issue: There is a potential issue regarding the service handles for the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis(TM) Anesthesia Station 4000 Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis" Anesthesia Station ES Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation 4000 System Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Potential...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower Recalled by CareFusion...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.