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. 2,563 recalls have been distributed to West Virginia in the last 12 months.
Showing 2141–2160 of 48,376 recalls
Recalled Item: Medshape Universal Joints Recalled by Medshape, INC. Due to Bone external...
The Issue: Bone external fixation system may have the pin that can become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Recalled...
The Issue: Due to a risk of false positive results that could lead to unnecessary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inseego USB8 4G Dongle Kit Recalled by Remote Diagnostic Technologies Ltd....
The Issue: Kit USB flash drive contains outdated software, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...
The Issue: Potential for inaccurate measurement of the patient circuit compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentamicin Injection Recalled by Eugia US LLC Due to Failed Stability...
The Issue: Failed Stability Specifications: Out of specification results for the Color...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Macleods Pharmaceuticals Ltd Due to...
The Issue: Presence of a foreign substance: black hair found embedded in tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectral CT. Computed tomography X-ray system. Recalled by Philips North...
The Issue: Devices with affected software may experience two unintended motion issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva IT Nova Product Number: 781175 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Product Number: 781106 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Due to identified...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR Product Numbers: (1) 781153 Recalled by Philips North America Due...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Ophthalmic Solution Recalled by Apotex Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.