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. 2,453 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,453 in last 12 months

Showing 2704127060 of 28,579 recalls

Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: Electrosurgical Tip Cleaner Recalled by ConMed Corporation Due to ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode Recalled by ConMed Corporation Due to...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ABC(R) NOZZLE Recalled by ConMed Corporation Due to ConMed received...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Needle with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· Stryker Spine

Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...

The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Blade with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· Integra LifeSciences Corp.

Recalled Item: MAYFIELD¿ Composite Series Base Unit Standard Recalled by Integra...

The Issue: Integra determined there is a possibility that the Base Units may break...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE MOIST Brand Contact Lenses Recalled by Johnson & Johnson Vision...

The Issue: Limited number of individual contact lens packages may not have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Limited number of individual contact lens packages may not have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· NordicNeuroLab AS

Recalled Item: nordicBrainEX Product Usage: nordicBrainEx is an image processing software...

The Issue: There is an error related to the relative geometry between fiber tracts in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Concentric Medical Inc

Recalled Item: FlowGate Balloon Guide Catheter Recalled by Concentric Medical Inc Due to...

The Issue: Firm received complaints of resistance and possible collapse of the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...

The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Philips Healthcare received reports from the field stating the patient table...

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

Class II — Potential Health HazardOngoing