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. 2,413 recalls have been distributed to Utah in the last 12 months.
Showing 38341–38360 of 49,677 recalls
Recalled Item: Taco Seasoning No Salt Recalled by Regency Group, Inc., The Due to Taco...
The Issue: Taco Seasoning No Salt is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Turtle Island Roast Beef Spice Blend Recalled by Regency Group, Inc., The...
The Issue: Turtle Island Roast Beef Spice Blend is recalled due to contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pizza Seasoning Recalled by Regency Group, Inc., The Due to Pizza Seasoning...
The Issue: Pizza Seasoning is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: James Gang BBQ Bull Breath Chili Seasoning Recalled by Regency Group, Inc.,...
The Issue: James Gang BBQ Bull Breath Chili Seasoning is recalled due to contamination...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Seasoning Suprema Recalled by Regency Group, Inc., The Due to Taco...
The Issue: Taco Seasoning Suprema is recalled due to contamination with gluten (wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EZ's Burger Deluxe -Burger Blend w/o MSG Recalled by Regency Group, Inc.,...
The Issue: EZ's Burger Deluxe -Burger Blend w/o MSG is recalled due to contamination...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Metro Market Lemon Pepper Rub Recalled by Regency Group, Inc., The Due to...
The Issue: Metro Market Lemon Pepper Rub is recalled due to contamination with gluten...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...
The Issue: Sterility of device maybe compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...
The Issue: complaints of system malfunction and unintended, sudden movement at start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...
The Issue: Potential for uncured adhesive between the metal threaded insert and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azithromycin Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin 500 mg tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Abnormal Power Source Switching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...
The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.