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. 1,060 recalls have been distributed to West Virginia in the last 12 months.
Showing 6981–7000 of 27,884 recalls
Recalled Item: VERIFY Steam Test Pack (20 Tests and 5 controls) Item Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...
The Issue: Biological indicator (BI) used to promote growth of the G....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...
The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc Host 2 as follows: Product SMN epoc Host 10736387 Recalled by Siemens...
The Issue: pO2 High Recovery in Quality Control When Adjusted for Barometric Pressure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...
The Issue: There is an increased chance that the tests from affected lots may give...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...
The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball bearings...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Trilogy 100 Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: The replacement silicone sound abatement foam installed into some Trilogy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: CENTURION MEDICAL PRODUCTS L & D TRAY...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE CABG PACK Recalled by MEDLINE...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE PAIN TRAY Recalled by MEDLINE...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Shoulder System Resection Planer 35mm Resection Planer Recalled by...
The Issue: Two planers were found to be unusable during sawbones shoulder training.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.