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. 2,495 recalls have been distributed to Utah in the last 12 months.
Showing 20781–20800 of 28,579 recalls
Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra operative MRI Systems: Neuro II-SE Recalled by Deerfield Imaging Due...
The Issue: Emergency helium venting lines (i.e. quench lines) may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: A report can be confirmed with the incorrect patient demographics resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device Recalled by...
The Issue: MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...
The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration...
The Issue: Complaints that the cannula bent/broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Series Stretchers (Fifth Wheel Recalled by Stryker Medical Division of...
The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transport Stretcher Recalled by Stryker Medical Division of Stryker...
The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Computed Tomography X-ray Systems Recalled by Philips...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Knee System Porous Femoral Component various sizes and Recalled...
The Issue: The anterior/posterior (AP) dimension may be oversized by 0.016 . If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.