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. 1,034 recalls have been distributed to West Virginia in the last 12 months.
Showing 14241–14260 of 48,376 recalls
Recalled Item: Strophanthus hisp 30X Recalled by Washington Homeopathic Products, Inc. Due...
The Issue: Out-of-specification test results obtained for identification testing based...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZTE 1015 Formula Recalled by Washington Homeopathic Products, Inc. Due to...
The Issue: Out-of-specification test results obtained for identification testing based...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Donepezil HCL Tablets Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone Hydrochloride Tablets Recalled by Rhodes Pharmaceuticals, L.P. Due...
The Issue: Presence of Foreign Tablets/Capsules; A single foreign tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trulicity (dulaglutide) Recalled by Eli Lilly & Company Due to Labeling:...
The Issue: Labeling: Label error on declared strength - autoinjector devices labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...
The Issue: Battery system data issue with the ultrasound system can intermittently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound Inc Due to Battery system...
The Issue: Battery system data issue with the ultrasound system can intermittently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641 Recalled by...
The Issue: The rear heater plate and cover assembly that contains the electrical wiring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scrip Creme All Purpose Lotion Intended for use in acoustic Recalled by...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scrip Ultrasound Gel Clear Recalled by Scrip Inc Due to Ultrasound gels and...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed tomography x-ray systems with software syngo.CT VA20A_SP4a Recalled...
The Issue: Software versions may result in sporadic problems causing scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoLink Bone Graft Harvester Recalled by In2bones USA, LLC Due to Complaints...
The Issue: Complaints were received of CoLink Bone Graft Harvesters breaking at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVENA PICC Sleeve Recalled by Queen Comfort Products lLC Due to Marketed...
The Issue: Marketed without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spironolactone Ophthalmic Solution 0.005 mg/mL Recalled by Prescription Labs...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X RATED HONEY FOR MEN Recalled by Phe Inc Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocky Top Farms Cherry Butter sold in 1 gallon food Recalled by Rocky Top...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EVIS EXERA BF-XT160 Bronchofibervideoscope Recalled by Olympus Corporation...
The Issue: A gluing step was not performed during the manufacturing of the affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-N20 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-XP60 OES Bronchofiberscope Recalled by Olympus Corporation of the...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-Q180-AC EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.