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. 2,318 recalls have been distributed to West Virginia in the last 12 months.
Showing 36261–36280 of 48,376 recalls
Recalled Item: WESTBROOK'S CANNERY HOT DILL PICKLES Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: West brook's Dilly Beans Recalled by Westbrook's Cannery Due to Products...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY DILL PICKLES Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Westbrook's Horseradish Dilly Beans Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4C Occiput Torque Wrench F/Set Screw Recalled by Aesculap, Inc. Due to A...
The Issue: A FW103R torque wrench that was improperly reassembled after reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX850 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce GX540 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX650 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from:...
The Issue: Subpotent Drug: menthol and methyl salicylate below specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SENSE Body Coil 1.5T with identification Recalled by Philips Electronics...
The Issue: Wrong positioning of the coil cables can create unintended resonances via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actuator for angiographic x-ray monitor ceiling suspension system. Actuator...
The Issue: The actuator assembly became detached and the monitor carriage with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Potential...
The Issue: Potential issue leading to data loss and patient data mix-up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....
The Issue: Product marketed without a 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicICE v 2.3.14 nordicICE is an image processing software package...
The Issue: The bug causes BOLD activation maps to be visualized as overlays without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...
The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.