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. 2,466 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,466 in last 12 months

Showing 2574125760 of 28,579 recalls

Medical DeviceAugust 27, 2013· Siemens Healthcare Diagnostics

Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Zimmer, Inc.

Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...

The Issue: Possibility of the weld to the quick-connect breaking when force is applied...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Snug Seat Inc

Recalled Item: Crocodile (size 3) are two-armed Recalled by Snug Seat Inc Due to The bolts,...

The Issue: The bolts, which secure the handles, on the Crocodile (size 3) could break,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Biomet 3i, LLC

Recalled Item: Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens...

The Issue: Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...

The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2013· Bayer Healthcare Llc

Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...

The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2013· Medtronic Xomed, Inc.

Recalled Item: Universal Titanium Prosthesis Recalled by Medtronic Xomed, Inc. Due to One...

The Issue: One lot of the product was assembled using the Cam Head version of the same...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2013· Becton Dickinson & Company

Recalled Item: BD Epilor Syringe BD Franklin Lakes Recalled by Becton Dickinson & Company...

The Issue: BD has received several reports indicating that the plunger of the 7 mL BD...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· Trans American Medical, Inc.

Recalled Item: Spectre Wireless Footswitch/Handswitch system Model 98/99 Recalled by Trans...

The Issue: TransAmerican Medical Imaging is recalling certain lots of TMI Spectre...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· ITC-Nexus Dx

Recalled Item: Surgicutt fully automated incision making device for bleeding time...

The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2013· Ebi, Llc

Recalled Item: BIOMET Spine Recalled by Ebi, Llc Due to Polaris Translation Screw Failures...

The Issue: Polaris Translation Screw Failures were recently reported to Biomet Spine....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Urine Combo 4 Sold outside of US Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 1 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Combo 3 Sold outside of US only. Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.33 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Breakpoint Combo 4 Sold outside of US Recalled by...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing