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. 2,563 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,563 in last 12 months

Showing 1610116120 of 28,579 recalls

Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· GE Healthcare Japan Corporation

Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...

The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Roche Diagnostics Corporation

Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...

The Issue: The device may give a falsely elevated result that is non-reproducible. If...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Roche Diagnostics Corporation

Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...

The Issue: The device may give a falsely elevated result that is non-reproducible. If...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Tibial Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing