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. 1,101 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
1,101 in last 12 months

Showing 9221–9240 of 28,579 recalls

Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A902416 Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2021· C.R. Bard Inc

Recalled Item: Catalog A303416A Recalled by C.R. Bard Inc Due to There is potential for...

The Issue: There is potential for packaging defects that may impact the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System...

The Issue: Customers have reported an increased number of false positive SARS-CoV-2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Abbott Molecular, Inc.

Recalled Item: Vysis CLL FISH Probe Kit with the following components: Vysis Recalled by...

The Issue: Potential for Vysis CLL FISH Probe Kits not detecting 13q deletions in known...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Mac Medical Supply Co Inc

Recalled Item: Ultrasound Gel labeled under the following brand names: MediChoice...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2021· Cardinal Health

Recalled Item: Monoject 0.9% Sodium Chloride Flush Syringe Recalled by Cardinal Health Due...

The Issue: Potential for the plunger to draw back after the air has been expelled and...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 3, 2021· Olympus Corporation of the Americas

Recalled Item: Arc Endocuff Vision as follows: ARV110 ENDOCUFF-V M BLUE PK8 Recalled by...

The Issue: Packaging seal defect may allow a breach of the package sterile barrier and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Luminex Corporation

Recalled Item: Verigene EP Amplification Reagent Kit Test Recalled by Luminex Corporation...

The Issue: There is potential for false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus Water Purification System Recalled by Fresenius Medical Care...

The Issue: AquaBplus HF module on the AquaBplus 2000 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uEXPLORER PET/CT System - Product Usage: intended to be operated Recalled by...

The Issue: The EXAM acquisition workflow could occasionally freeze after canceling the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD SmartSite 'Y' Extension Set 2 Needle-Free Valves Recalled by CAREFUSION...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· Magnolia Medical Technologies, Inc.

Recalled Item: Steripath Luer Transport Pack Recalled by Magnolia Medical Technologies,...

The Issue: Product was shipped with the incorrect Transfer Adapter Instructions For Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity Burette Set 60 DP 3 SmartSite VALVES BALL VALVE DRIP CHAMBER...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD ADD-ON Burette Set V/NV Needle-Free Valve Recalled by CAREFUSION Due to...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity IV Set 3-port Closed Manifold Back Check Valve 3 Needle-Free...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD BURETTE GRAVITY SET 60 DROP 2 Smartsite VALVES VENTED/NONVENTED Recalled...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2021· CAREFUSION

Recalled Item: BD Extension Set SMALLBORE Tubing SmartSite VALVE Recalled by CAREFUSION Due...

The Issue: Needle-free connector valves, either standalone or attached to extension...

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

Class II — Potential Health HazardOngoing