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. 2,450 recalls have been distributed to Utah in the last 12 months.
Showing 32001–32020 of 49,677 recalls
Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...
The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: due to out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance ICT SP Computed Tomography X-ray system Recalled by Philips...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT Computed Tomography X-ray system Recalled by Philips...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...
The Issue: The product label does not include the correct current rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...
The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ben & Jerrys Brownie Batter Core Ice Cream One Pint Recalled by Unilever...
The Issue: Certain pints of Ben & Jerrys Brownie Batter Core Ice Cream may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...
The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...
The Issue: Encoded with incorrect ranges that are not consistent with the ranges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...
The Issue: Potential presence of particulate matter on the blood side of the dialyzer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roland¿ Preserved Lemons Recalled by Roland Foods, LLC. Due to Undeclared...
The Issue: The product contains undeclared sulfites based on sampling and analysis by...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Algovita Spinal Cord Stimulation System Recalled by Nuvectra Due to Nuvectra...
The Issue: Nuvectra is conducting a recall due to two clinical risks that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...
The Issue: An error may occur with the display of dose computed on images other than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.