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. 2,623 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,623 in last 12 months

Showing 96019620 of 28,579 recalls

Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: TruRize Clinical Chair - support structure that places human occupants...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Isolibrium Support Surface - support surface assists in the prevention...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime TC-transport chair intended for medical purposes to assist a Recalled...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Encore Medical, LP

Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...

The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Encore Medical, LP

Recalled Item: DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus Recalled by Encore...

The Issue: Packaging mixup; There is a potential that packaging identified as 12mm knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Exactech, Inc.

Recalled Item: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT....

The Issue: The HAT trial contains a retaining ring that has shown the potential to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: novaplus Recalled by Medical Action Industries, Inc. 306 Due to There is a...

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Recalled by Medical Action Industries, Inc....

The Issue: There is a potential for flaking metal and/or brown spots on the hemostats...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2021· Skytron, Div. The KMW Group, Inc

Recalled Item: Skyton Bracket Flatscreen Recalled by Skytron, Div. The KMW Group, Inc Due...

The Issue: Failure of the FS32 Monitor Brackets from the mounting block could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Randox Laboratories Ltd.

Recalled Item: NEFA CAL (Non-Esterified Fatty Acids)- IVD Standard for measurement of...

The Issue: Standard packed within NEFA kit has been assigned incorrectly. Calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· IMPLANTCAST GMBH

Recalled Item: EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit...

The Issue: A risk exists during impacting of the acetabular cup into the bone the plugs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· Ventec Life Systems, Inc.

Recalled Item: Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog...

The Issue: Due to a component failure, ventilators may unexpectedly shut down or have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2021· BioFire Diagnostics, LLC

Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to Elevated...

The Issue: Elevated rates of false negative results may occur when using blood culture...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 Recalled by...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare Plus Blood Lead Test Kit Catalog Number 82-0004 Recalled by...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2021· Magellan Diagnostics, Inc.

Recalled Item: LeadCare II Blood Lead Test Kit Catalog Number 70-6762 Recalled by Magellan...

The Issue: Magellan has received reports that control tests of either the Low-Control...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2021· K2M, Inc

Recalled Item: Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2...

The Issue: Mislabeled product labeling incorrect length or height, or length and height...

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

Class II — Potential Health HazardOngoing