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. 2,595 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,595 in last 12 months

Showing 1192111940 of 28,579 recalls

Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab Start.Kit LT - ceramic Recalled...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - Recalled by...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing