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. 2,530 recalls have been distributed to West Virginia in the last 12 months.
Showing 6861–6880 of 27,884 recalls
Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...
The Issue: Incorrect expiration date on product label. The manufacturing date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...
The Issue: Firm identified that user may be unable to adjust the length of the Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter...
The Issue: Due to the adhesive provided within the catheter repair kits maybe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR Recalled by...
The Issue: Gauge malfunction: Digital gauge displays an incorrect tank pressure -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Medline Sterile Hand Pack Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The convenience trays had improper placement of some of the components that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sterile Oncology Port Access Tray Recalled by MEDLINE INDUSTRIES, LP...
The Issue: The convenience trays had improper placement of some of the components that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Medline Sterile Maximum Barrier Pack-LF Recalled by MEDLINE INDUSTRIES,...
The Issue: The convenience trays had improper placement of some of the components that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Recalled by Philips Healthcare (Suzhou) Co., Ltd. Due to...
The Issue: Multiple software issues which have the potential to lead to misdiagnosis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8 Recalled by...
The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 Recalled by...
The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Delivery Set with Filter Recalled by Quest Medical, Inc. Due to...
The Issue: Delivery Sets may have tubing that could become detached that could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTURION MEDICAL PRODUCTS Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: The kit contained an expired component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short Recalled...
The Issue: Product Mislabeled on the outer bag and inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- Recalled by...
The Issue: Anti-HBe2 (aHBe2) interference with the Hepatitis B e Antigen (HBeAg) Assay,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term...
The Issue: Label with the incorrect component listed on the inner kit Tyvek header bag
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Covera Vascular Covered Stent is a flexible Recalled by Bard Peripheral...
The Issue: An increase in the reported complaint rate for inability to deploy was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RipCord Syndesmosis Button Recalled by TriMed Inc. Due to Overly aggressive...
The Issue: Overly aggressive tension on the pull suture, while passing the medial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE DRILL BIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: The recall is due to observed intra-operative screw failure. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.