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 38121–38140 of 49,677 recalls
Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide capsules Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotidine tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clarithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to Non-invasive...
The Issue: Non-invasive blood pressure pumps (NIBP) voltage is not sufficient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nice! Powdered Sugar Mini Donuts 11.5 oz packaged in a Recalled by Walgreen...
The Issue: Nice! Powdered Sugar Mini Donuts may contain mold. Alleged illnesses have...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....
The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 530. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph. The ELI 380 is intended to be a high-performance...
The Issue: Mortara Instrument, Inc. has recently become aware of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite 200 in vitro diagnostic. Product Usage: The Tecan Infinite Recalled...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite M1000 in vitro diagnostic. Product Usage: The Tecan Infinite...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.