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. 2,639 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,639 in last 12 months

Showing 61416160 of 49,677 recalls

Medical DeviceApril 5, 2024· Randox Laboratories Ltd.

Recalled Item: Evidence MultiSTAT with software v 3.7-Analyzer intended for the qualitative...

The Issue: Foam gasket on the Evidence MultiSTAT chip heater assembly may not perform...

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

Class III — Low RiskOngoing
Medical DeviceApril 5, 2024· IVOCLAR VIVADENT AG

Recalled Item: IPS e.max ZirCAD CER/in. Prime A3 C17/5 -A zirconium oxide Recalled by...

The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2024· IVOCLAR VIVADENT AG

Recalled Item: IPS e.max ZirCAD CER/in. Prime C2 C17/5- A zirconium oxide Recalled by...

The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2024· IVOCLAR VIVADENT AG

Recalled Item: IPS e.max ZirCAD CER/in. Prime BL1 C17/3- A zirconium oxide Recalled by...

The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2024· IVOCLAR VIVADENT AG

Recalled Item: IPS e.max ZirCAD CER/in. Prime A2 C17/5 -A zirconium oxide Recalled by...

The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2024· IVOCLAR VIVADENT AG

Recalled Item: IPS e.max ZirCAD CER/in. Prime B1 C17/5 -A zirconium oxide Recalled by...

The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2024· IVOCLAR VIVADENT AG

Recalled Item: IPS e.max ZirCAD CER/in. Prime A1 C17/5 - A zirconium Recalled by IVOCLAR...

The Issue: Defective blocks may show cracks after sintering If cracks are unnoticed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2024· Philips Medical Systems Nederland B.V.

Recalled Item: Philips IntelliSpace Cardiovascular software Recalled by Philips Medical...

The Issue: Study data is not able to be archived, copied, or exported with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2024· Stryker Leibinger GmbH & Co. KG

Recalled Item: 8000-021-002 Recalled by Stryker Leibinger GmbH & Co. KG Due to Unreleased...

The Issue: Unreleased software was installed on customer systems resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2024· Macherey Nagel Gmbh & Co. Kg

Recalled Item: Reagent Test Strips for Blood Recalled by Macherey Nagel Gmbh & Co. Kg Due...

The Issue: The reason for the recall is one of the test pads, for the parameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2024· Olympus Corporation of the Americas

Recalled Item: InstaClear Lens Sheath. The InstaClear lens cleaner system and versatile...

The Issue: Potential for distal end of the sheath to break off during a procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2024· Stryker Neurovascular

Recalled Item: The Distal Access Catheter is a single-lumen Recalled by Stryker...

The Issue: Stryker Neurovascular is recalling their DAC- Distal Access Catheter -038...

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

Class II — Potential Health HazardOngoing
FoodApril 2, 2024· Taylor Farms Southwest, Inc

Recalled Item: Family Size Garden Salad 17oz packaged in Flexible plastic combo Recalled by...

The Issue: On 03/30, TFSW ALBSWY CHICKEN CAESAR SALAD 10OZ (Egg, F-Anchovy, Milk, Soy,...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2024· X-Gen Pharmaceuticals Inc.

Recalled Item: Cyclophosphamide for Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Incorrect or missing Package Insert: There is an error on the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 2, 2024· X-Gen Pharmaceuticals Inc.

Recalled Item: Cyclophosphamide for Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Incorrect or missing Package Insert: There is an error on the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 2, 2024· Agilent Technologies

Recalled Item: Brand Name: Dako CoverStainer Recalled by Agilent Technologies Due to There...

The Issue: There is the potential for the front plexiglass door of the automated slide...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2024· Andover Healthcare Inc.

Recalled Item: Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage Recalled by Andover...

The Issue: A packaging seal gap could impact the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2024· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Airvo 2 Humidifier Recalled by Fisher & Paykel Healthcare, Ltd. Due to...

The Issue: Humidifier devices, used to deliver high flow respiratory therapy to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2024· Philips Respironics, Inc.

Recalled Item: OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124...

The Issue: Device may experience an interruption or loss of therapy in case of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2024· Karl Storz Endoscopy

Recalled Item: LASER Application Instrument Recalled by Karl Storz Endoscopy Due to Laser...

The Issue: Laser surgical instruments have no specific evidence of a validated...

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

Class II — Potential Health HazardOngoing