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. 2,450 recalls have been distributed to West Virginia in the last 12 months.
Showing 18141–18160 of 27,884 recalls
Recalled Item: Two-Lumen Hemodialysis Catheterization Kit with Blue Flex Tip(R) Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable PICC Kit The Arrow International Pressure...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High...
The Issue: The large-bore two-lumen catheter permits venous access to the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickFlash Radial Artery/Arterial Line Catheterization Kit The Arrow¿...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology...
The Issue: When the Smart Check tool is used to perform a Smart Setup with one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit. The large-bore...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ Administration Set Recalled by Smiths Medical ASD Inc. Due to Smiths...
The Issue: Smiths Medical has become aware that the drawing on the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Estradiol II Recalled by BioMerieux SA Due to Fulvestrant cross reacts...
The Issue: Fulvestrant cross reacts with the VIDAS Estradiol II immunoassay and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation Recalled...
The Issue: Medtronic received reports that the DBS depth stop did not adequately secure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRK Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes Recalled...
The Issue: BD is initiating this product correction of multiple lots of BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrectomy Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cataract Kit - Dr. Slingsby Recalled by Windstone Medical Packaging, Inc....
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ophthalmic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.