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. 2,466 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,466 in last 12 months

Showing 2452124540 of 49,677 recalls

Medical DeviceAugust 15, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...

The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...

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

Class II — Potential Health HazardOngoing
DrugAugust 14, 2018· Mckesson Corporation

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Corporation Due to...

The Issue: Supterpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2018· AVKARE Inc.

Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2018· AVKARE Inc.

Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2018· AVKARE Inc.

Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2018· AVKARE Inc.

Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 14, 2018· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...

The Issue: Failed Impurities/Degradation Specifications; out of specification results...

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

Class III — Low RiskOngoing
Refund
FoodAugust 14, 2018· SALT & STRAW LLC

Recalled Item: Chocolate Gooey Brownie Ice Cream Recalled by SALT & STRAW LLC Due to...

The Issue: Chocolate Gooey Brownie Ice Cream is recalled due to possible undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 14, 2018· Tec Com Gmbh

Recalled Item: TECOTHERM NEO Recalled by Tec Com Gmbh Due to The action is being initiated...

The Issue: The action is being initiated due to potential installation of faulty...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2018· Ohio Medical Corporation

Recalled Item: Portable Suction Pump Recalled by Ohio Medical Corporation Due to The...

The Issue: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2018· Stryker Spine

Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...

The Issue: The anterior and posterior markers on the cage were on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2018· bioMerieux, Inc.

Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...

The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2018· bioMerieux, Inc.

Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...

The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...

The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2018· The Binding Site Group, Ltd.

Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...

The Issue: A deterioration of performance was identified with influenza type B Enzyme...

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

Class II — Potential Health HazardOngoing
DrugAugust 10, 2018· Westlab Pharmacy, Inc. dba Westlab Pharmacy

Recalled Item: Cyclosporine 1% Human Eye Drops Recalled by Westlab Pharmacy, Inc. dba...

The Issue: Lack of Process Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2018· Westlab Pharmacy, Inc. dba Westlab Pharmacy

Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...

The Issue: Lack of Process Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2018· Westlab Pharmacy, Inc. dba Westlab Pharmacy

Recalled Item: Alprostadil 500 mcg/mL Injectable Recalled by Westlab Pharmacy, Inc. dba...

The Issue: Incorrect Product Formulation

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2018· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...

The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.

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

Class III — Low RiskOngoing
DrugAugust 9, 2018· Orexigen Therapeutics, Inc.

Recalled Item: Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets...

The Issue: Defective Container: Customer complaints of punctures in the bottle.

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

Class III — Low RiskOngoing
Refund