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. 2,361 recalls have been distributed to Utah in the last 12 months.
Showing 47661–47680 of 49,677 recalls
Recalled Item: American Vines band Natural Vines Black Soft Licorice Twists Recalled by...
The Issue: Firm's internal sampling of the product found elevated levels of lead in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Variety and Assortment Packs containing Frosted/ Unfrosted Mini...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Frosted Mini Wheats Recalled by Kellogg Company Due to This...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Canadian Product: Kellogg's Mini Wheats Recalled by Kellogg Company Due to...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Mini Wheats Recalled by Kellogg Company Due to This voluntary...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...
The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...
The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178...
The Issue: Broken screw insertor hardness was measured and found to be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride...
The Issue: CGMP Deviations: The products were manufactured with raw material which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fairytale Brand Peanut Butter Sprites Recalled by Fairytale Brownies, Inc...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brownies Brand Peanut Butter Brownies Recalled by Fairytale...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fairytale Brownies Brand Peanut Butter Cookies Recalled by Fairytale...
The Issue: The firm initiated voluntarily recall because the products contains peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Late July Organic Mini Peanut Butter Sandwich Crackers packaged in Recalled...
The Issue: Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...
The Issue: Potential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...
The Issue: Potiential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Philips Medical Systems...
The Issue: Philips is issued a Field Change Order to update Extended Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...
The Issue: The insert provided with the product for the specific lot number indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.