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 2576125780 of 28,579 recalls

Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Breakpoint Combo 7 Product Usage:...

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 Combo 2 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 Synergies Plus Negative Urine Combo 2 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 20, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX Evolution System (Standard Q) The DRX-Evolution System...

The Issue: Carestream received a report of an exposure being initiated without a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHECK FastClix Lancing Device. It is intended for use in Recalled by...

The Issue: Internal Roche inspections have revealed that after the lancet is used for a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Intact PTH Calibrator (6 pack) Recalled by Siemens Healthcare...

The Issue: PTH Calibrator packaged with only high calibrator.

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

Class III — Low RiskOngoing
Medical DeviceAugust 16, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT Diagnostic imaging system for fixed or mobile Recalled...

The Issue: Issues with the Ingenuity TF PET/CT Software Version 4.0 could pose a risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 10 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Covidien LLC

Recalled Item: Monoject 100 Units/mL Heparin Lock Flush Recalled by Covidien LLC Due to...

The Issue: Monoject prefill flush syringes may contain non-sterile water and labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S Recalled by Siemens Medical Solutions USA, Inc. Due to The...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia T Series SPECT + CT Product Usage 1) SPECT: Recalled by Siemens...

The Issue: The detectors on the Symbia S and Symbia T camera systems are supported and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO - Beam shaping block for Radiation Therapy. Recalled by Elekta,...

The Issue: Clinical mistreatment may occur when there are errors in the clinical...

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

Class II — Potential Health HazardOngoing