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. 2,453 recalls have been distributed to Utah in the last 12 months.
Showing 30441–30460 of 49,677 recalls
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18L6 HD transducer on the ACUSON S Family ultrasound systems Recalled by...
The Issue: When scanning with the 18L6 HD transducer on the ACUSON HELX" Evolution with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alka-Seltzer Original ( 325 mg Aspirin (NSAID) Recalled by Bayer HealthCare...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID) Recalled by Bayer...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alka-Seltzer Gold (1000 mg Anhydrous citric acid Recalled by Bayer...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors....
The Issue: If metal strips are removed and re-applied to another display, there is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some...
The Issue: Some of the individual unit packaging (pouches) may be missing the lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Therm Hyper/Hypothermia System Recalled by Stryker Medical Division of...
The Issue: The water may reheat too quickly if the unit is in "Automatic" mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...
The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE426R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: hCG Body Shaper Recalled by Gary Wood Due to Marketed without an Approved...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis has found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Taro Pharmaceuticals...
The Issue: Failed Content Uniformity Specifications; out-of-specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.