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. 1,744 recalls have been distributed to Utah in the last 12 months.
Showing 47921–47940 of 49,677 recalls
Recalled Item: 1/4" Slivered Yellow Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/4" Diced Red Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/2" Diced Yellow Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 3/16" Slivered Red Onions Recalled by Gills Onions, LLC Due to Potential...
The Issue: Gills Onions is recalling diced and slivered onions because it may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: florAlign Prebiotic Formula Recalled by Eco Health, Inc. Due to Potential...
The Issue: Eco Health is recalling florAlign Prebiotic Formula because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste...
The Issue: CGMP Deviations: Product was made with an incorrect ingredient, Laureth-9...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...
The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...
The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...
The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Ball taper for humeral stem Recalled by Zimmer, Inc....
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLS Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Ventralight ST Mesh. - Ellipse 7" x 9" (17.8 Recalled by Davol, Inc.,...
The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DTO" Implant Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw Recalled by...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 Recalled by Davol, Inc.,...
The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...
The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alloclassic SL Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.