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. 2,507 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,507 in last 12 months

Showing 1906119080 of 28,579 recalls

Medical DeviceDecember 2, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...

The Issue: Edits to Particle field definition parameters may not be saved when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...

The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...

The Issue: Reunion TSA Peg Alignment Sound broke during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· K2M, Inc

Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...

The Issue: Instruments were developed without adequate consideration given to the need...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: A1CNow+ Systems (professional use product) Recalled by Polymer Technology...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: CVS Health At Home A1C Test Kit Recalled by Polymer Technology Systems Due...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: Walgreens At-Home A1C Test Kit Recalled by Polymer Technology Systems Due to...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: A1CNow SELF CHECK (European) Recalled by Polymer Technology Systems Due to A...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Polymer Technology Systems

Recalled Item: ReliOn FastA1C Test Recalled by Polymer Technology Systems Due to A...

The Issue: A numerical value less than 4% or greater than 13% may be displayed instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Merit Medical Systems, Inc.

Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...

The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2016· Pride Mobility Products Corp

Recalled Item: TRU-Balance 3 Power Positioning Systems Recalled by Pride Mobility Products...

The Issue: The interface between the TB3 back and tilt base can separate when tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8470-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-530 3.0MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-009-030 3.0MM Precision Round Recalled by Stryker Instruments Div. of...

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2016· Ecolab Inc

Recalled Item: Ecolab Recalled by Ecolab Inc Due to The reason for the recall is that the...

The Issue: The reason for the recall is that the inner carton box of the Rolled Probe...

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

Class III — Low RiskOngoing
Medical DeviceNovember 30, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 8450-107-525 2.5MM Precision Match Head Recalled by Stryker Instruments Div....

The Issue: Stryker Instruments is voluntarily recalling specific lots of sterile MIS...

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

Class II — Potential Health HazardOngoing