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. 2,595 recalls have been distributed to Utah in the last 12 months.
Showing 13681–13700 of 28,579 recalls
Recalled Item: REVACLEAR 400 Dialyzer Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVACLEAR 300 Dialyzer Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEO Patient Monitor /Tranquility VS Patient Monitor Recalled by Infinium...
The Issue: The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Tray Nonporous A Size 2 Recalled by Ortho Development Corporation Due...
The Issue: The locking mechanism of the tibial tray exhibited a manufacturing defect in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Tray Nonporous A Size 4 Recalled by Ortho Development Corporation Due...
The Issue: The locking mechanism of the tibial tray exhibited a manufacturing defect in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...
The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...
The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...
The Issue: Additional Instructions: step-by step handling and inserting the cassette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...
The Issue: Potential for increased rate of false positive results and/or increased rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....
The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...
The Issue: Packaged dental implant healing abutments were found to contain the wrong...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ICS CHARTR EP 200 Recalled by GN Otometrics Due to There is a risk to...
The Issue: There is a risk to the healthcare professional or patient of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.