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. 2,460 recalls have been distributed to West Virginia in the last 12 months.
Showing 16221–16240 of 27,884 recalls
Recalled Item: clariti 1 day (-1.25) 90 pack Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F-T3SYSTEM Recalled by Allen Medical Systems Due to The recalling firm has...
The Issue: The recalling firm has become aware that the rail section clamps used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-4.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution Recalled by Draegar...
The Issue: The invasive pressure visual and audible alarms may not activate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clariti 1 day/Fresh Day 90 pack (-1.00) Recalled by CooperVision Inc. Due to...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: True 3D Viewer Recalled by Echopixel, Inc. Due to With certain software...
The Issue: With certain software versions, import of enhanced ultrasound formatted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource PBDS Recalled by Cardinal Health 200, LLC Due to A defect in the...
The Issue: A defect in the seal of the Gatorade pouch contained in kits caused the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza software VB10A model numbers: 10863171 Recalled by Siemens...
The Issue: Software upgrade to correct format of study dates and issues with Legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza software Syngo.Plaza is a Picture Archiving and Communication...
The Issue: Software upgrade to correct format of study dates and issues with Legacy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini...
The Issue: Lack of adequate validation and controls to ensure that product cleanliness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable...
The Issue: Lack of adequate validation and controls to ensure that product cleanliness...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doyen-Collin Mouth Gag 120MM/ General Instruments Recalled by Aesculap...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strauss Penis Clamp 130MM/General Instruments Recalled by Aesculap Implant...
The Issue: The plastic sleeves of the Penis Clamp and Mouth Gag may stick together...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic ADT1018 Flow QC Clear Advantage Tubing Recalled by Transonic...
The Issue: The sterility of the device cannot be assured. There is a potential for an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Following a period of inactivity, the mass storage device may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M2 / PRIMUS Mid-Energy Recalled by Siemens Medical Solutions USA,...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Impression Plus Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Control Console software has been updated to reduce the risk for collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.