Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,356 recalls have been distributed to West Virginia in the last 12 months.
Showing 27201–27220 of 27,884 recalls
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System is a computed Tomography X-ray...
The Issue: One of the four screws that secure the Oil-accumulator to the X-Ray Tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune Bronze Rover Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker has received two reports of serious injury as a result of tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Procedural Trays: Merit's Custom Total Hip Pack Recalled by Merit...
The Issue: Custom Procedural trays contain Stryker Hytrel Togas which are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Shot Epidural Trays Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is recalling one lot of Single Shot Epidural Trays as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo(R) Lab Data Manager. The syngo(R) Lab Data Manager Recalled by...
The Issue: The recalling firm has discovered that when using a Sysmex(R) CA-7000 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink(TM) Informatics System Recalled by Siemens Healthcare Diagnostics,...
The Issue: There is a potential for the EasyLink system to display and transmit to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to Arrow is...
The Issue: Arrow is recalling the product due to the possibility of voids in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots...
The Issue: Siemens has confirmed that the Stratus(R) CS Acute Care(TM) D-Dimer CalPak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza radiological image processing system. Recalled by...
The Issue: Siemens became aware of an unintended behavior when using syngo.plaza. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Ultraview DM3 Monitor Model Number: 91330-NT The Ultraview DM3...
The Issue: Unit fails to power up, resulting in an equipment alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Rigid Suction Wand Recalled by Edwards Lifesciences,...
The Issue: Edwards is recalling Suction Wand models SPC2081 and S033 because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with Recalled by Sendx...
The Issue: The firm recalled because the glucose measurements from a patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The Tyvek pouch...
The Issue: The Tyvek pouch label for this device states: 'with holster'; however, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...
The Issue: Complaints have been reported where, during surgery, the surgeon was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The carton label for...
The Issue: The carton label for this device has the manufacturer symbol where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.