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. 2,543 recalls have been distributed to West Virginia in the last 12 months.
Showing 5381–5400 of 48,376 recalls
Recalled Item: Cathflo activase (ALTEPLASE) Recalled by Genentech, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Deformed stoppers observed during filling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Pfizer Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Labetalol Hydrochloride Injection Recalled by Pfizer Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tivicay PD (dolutegravir) 5mg Tablets for Oral Suspension Recalled by...
The Issue: Labeling: Incorrect Lot and/or Expiration Date: The carton has incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...
The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade Recalled...
The Issue: Cranial Caudal Blades manufactured incorrectly could result in fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Recalled by...
The Issue: Siemens Healthineers has identified an issue with the RAPIDPoint500e system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HemoPro Endoscopic Vessel Harvesting Systems are designed for...
The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stimuplex A Recalled by B Braun Medical Inc Due to The devices are labeled...
The Issue: The devices are labeled "not made with DEHP" or the DEHP free symbol;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System Recalled by...
The Issue: Potential for there to be a fluid ingress into the handle of the harvesting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RingLoc Bi-Polar Hip System Acetabular Cup Recalled by Biomet, Inc. Due to...
The Issue: 41 mm acetabular outer heads were potentially assembled with a 42 mm locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of Recalled by...
The Issue: Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 3028 Recalled by Inspire Medical Systems Inc. Due to There is...
The Issue: There is a potential manufacturing defect which can lead to electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...
The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Liberta RC Recalled by Abbott Medical Due to Deep brain stimulation...
The Issue: Deep brain stimulation system will first turn off after approximately 50...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.