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. 1,804 recalls have been distributed to West Virginia in the last 12 months.
Showing 22801–22820 of 48,376 recalls
Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEMBERS MARK SELF RISE FLR 25LB Recalled by Ardent Mills, LLC Due to...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB Recalled by Ardent Mills, LLC...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HILLTOP HEARTH SELF RISE FLR 25LB and 50LB Recalled by Ardent Mills, LLC Due...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARDENT H&R SR FLR Recalled by Ardent Mills, LLC Due to Potential Salmonella...
The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urethral Dilation Balloon Catheter with Open Tip Recalled by Cook Inc. Due...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.