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. 1,823 recalls have been distributed to Utah in the last 12 months.
Showing 38881–38900 of 49,677 recalls
Recalled Item: GLIPIZIDE and METFORMIN HYDROCHLORIDE Tablets Recalled by Heritage...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1:...
The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...
The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....
The Issue: Device software treatment preset parameters for the XC treatment handpiece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...
The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator...
The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...
The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...
The Issue: Customer reports that the ventilator display can freeze. Ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 5/20 sulfite-free (5% amino-acid with electrolytes in 20%...
The Issue: Lack of Assurance of Sterility; increased complaints received for leaks
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp Due to...
The Issue: Lack of Assurance of Sterility; increased complaints received for leaks
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sedecal SA Mobile Diagnost w DR x-ray system Recalled by Sedecal USA, Inc....
The Issue: Due to a software defect, the system may sporadically apply the default x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...
The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens internal investigation confirmed that current contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.