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.
Showing 23681–23700 of 49,677 recalls
Recalled Item: Medtronic Adapter Percutaneous Pin Recalled by Medtronic Navigation, Inc....
The Issue: Under certain circumstances, the percutaneous pin adapter used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon DUALSTOP Red Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vyon DUALSTOP White Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature...
The Issue: Some SureStep" Foley Tray Systems with product catalog number A319418AM and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-View¿ Contrast Enhanced Digital Mammography Recalled by Hologic, Inc. Due...
The Issue: Calibration issue not possible to visualize contrast uptake in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate 2 mcg per mL (200 mcg per 100 Recalled by Pharmedium...
The Issue: Sub-potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate 2 mcg per mL (100 mcg per 50 Recalled by Pharmedium...
The Issue: Sub-potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toothete Oral Care Sodium Bicarbonate Mouthpaste Recalled by Sage Products...
The Issue: A voluntary recall of a lot (67924) of Independent Care System due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...
The Issue: The sterility may be compromised due to a potential breach in the packaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Preserve Humeral Stem Recalled by Exactech, Inc. Due to Possibility...
The Issue: Possibility that the Equinoxe Preserve Humeral Stem, 8mm, was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol Tablets Recalled by Epic Pharma, LLC Due to Presence of foreign...
The Issue: Presence of foreign tablet/capsule: A single foreign tablet was found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diatomaceous Earth packaged in the following ways: 1) Perma-Guard Recalled...
The Issue: Product contains elevated levels of lead, arsenic, and chromium: potentially...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...
The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...
The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NYSTATIN Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Aurobindo Pharma USA...
The Issue: Discoloration: This product is being recalled due to a confirmed pharmacist...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.