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. 2,666 recalls have been distributed to Utah in the last 12 months.
Showing 1641–1660 of 28,579 recalls
Recalled Item: Dexcom G7 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium Needle-Free Syringe: 3 mL Recalled by BD SWITZERLAND SARL Due to...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Novum IQ Syringe Pump Recalled by Baxter Healthcare Corporation Due...
The Issue: Baxter has identified a design issue which may cause the pump to detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Recalled by Ortho-Clinical Diagnostics, Inc. Due to a...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...
The Issue: A software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: Description/: MNA-420 ENC -H/K9303320 Recalled by Barco N.V. Due to...
The Issue: Cathode ray tube display system encoders and decoders have same MAC address;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope...
The Issue: The replacement rechargeable batteries inserted into the Welch Allyn...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Product Name / UDI-DI code / Catalog No. Recalled by CareFusion...
The Issue: Antivirus software was not consistently installed on impacted devices during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name [REF]: Supply Server Recalled by CareFusion 303, Inc. Due to...
The Issue: During automated dispensing cabinet upgrade/installation/reimaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GCE HEALTHCARE Zen-O lite Recalled by Ohio Medical Corporation Due to...
The Issue: Erroneous calibration values, potentially resulting in: as the device ages,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Coil System /UDI-DI codes: PRES0153CXPPLT 00810068567311...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima Coil System /UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK...
The Issue: Due to radiopaque (RO) marker was not visible during angiography and it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.