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. 2,471 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,471 in last 12 months

Showing 2320123220 of 49,677 recalls

Medical DeviceFebruary 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...

The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2019· Luminex Corporation

Recalled Item: Aries Bordetella Assay Recalled by Luminex Corporation Due to Through...

The Issue: Through internal investigation, it was discovered that a portion of side...

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

Class II — Potential Health HazardOngoing
FoodFebruary 20, 2019· Meijer

Recalled Item: Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic Recalled...

The Issue: Undeclared soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2019· Beaver Visitec

Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...

The Issue: The product contains a misprinted expiration date on the peel pack. Both...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 19, 2019· The Binding Site Group, Ltd.

Recalled Item: Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive...

The Issue: Deterioration of C-reactive protein (CRP) reagent in Optilite C-Reactive...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· Philips Medical Systems Nederlands

Recalled Item: Foot Switches used with the following systems: 722001 Allura Xper Recalled...

The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· Philips Medical Systems Nederlands

Recalled Item: Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector...

The Issue: Additional units have been identified for previous recall Z-1280-2016 (RES...

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

Class II — Potential Health HazardOngoing
DrugFebruary 19, 2019· American Health Packaging

Recalled Item: Lovastatin Tablets USP Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
FoodFebruary 16, 2019· Concord Foods, LLC

Recalled Item: Concord Fresh Success Mild Salsa Seasoning Mix Recalled by Concord Foods,...

The Issue: Product contains undeclared allergen, milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nita Foods Inc.

Recalled Item: Nita Crisp Spelt Bread Cracker Recalled by Nita Foods Inc. Due to Undeclared...

The Issue: Nita Crisp Spelt Bread Cracker for undeclared wheat.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt....

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2019· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...

The Issue: The polarity of the output of power supply was reversed. Due to polarity of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2019· Covidien, PLC

Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...

The Issue: Potential for the sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
DrugFebruary 15, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Etomidate Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Subpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2019· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Dimercaptopropanesulfonate Sodium (DMPS) Recalled by McGuff Compounding...

The Issue: Presence of Particulate Matter: Particulates observed in vials release for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing