Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,404 recalls have been distributed to North Dakota in the last 12 months.
Showing 20021–20040 of 27,512 recalls
Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...
The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC unit because a component on the PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...
The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...
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: 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 Flu A/B & RSV Direct (MOL2650) 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: 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: Discovery ST Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightSpeed Plus (4-slice MDAS LightSpeed 4.0 CT Scanner System - Recalled by...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
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: 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: LightSpeed 16 (MDAS only Recalled by GE Medical Systems, LLC Due to GE...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
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: RediGuard IAB: 7Fr 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: 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: LightSpeed Ultra (8-slice MDAS) Recalled by GE Medical Systems, LLC Due to...
The Issue: GE Healthcare has updated the Service Manuals for a number of CT and PET CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 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: 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: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...
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.