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. 2,547 recalls have been distributed to West Virginia in the last 12 months.
Showing 4401–4420 of 48,376 recalls
Recalled Item: Bliss Tree Millet Butter Karasev 200g . Packaged in a box Recalled by Sri...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bliss Tree Moringa Butter Murukku 400g . Packaged in pouches Recalled by Sri...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bliss Tree Millet Butter Murukku 200g . Packaged in box Recalled by Sri...
The Issue: Undeclared sesame and milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bliss Tree Millet Butter Ribbon Pakoda 200g . Packaged in a box Recalled by...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bliss Tree Curry Leaves Butter Murukku 400g . Packaged in Recalled by Sri...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bliss Tree Ragi Butter Murukku 200g . Packaged in a box Recalled by Sri...
The Issue: Undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: American Outdoor Products - Astronaut Strawberries Recalled by American...
The Issue: Elevated levels of lead
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TIRZEPATIDE 60 mg/3mL (20/mg/mL) Recalled by ProRx LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TIRZEPATIDE 20 mg/2mL (10/mg/mL) Recalled by ProRx LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEMAGLUTIDE 10mg/4mL (2.5mg/mL) Recalled by ProRx LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tirzepatide 2 mL (10 mg/mL) and 20 mg/mL Recalled by ProRx LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by ProRx LLC Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL Recalled by ProRx LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEMAGLUTIDE 5mg/2mL (2.5mg/mL) Recalled by ProRx LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001 Recalled by Kinova...
The Issue: Potential installation issue that could result in a fire hazard in the event...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 App versions 1.3.0 and 1.3.2 Recalled by Medtronic...
The Issue: Due to two software anomalies that can occur within a spine procedure. Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen Series Reagent strips for Urinalysis are composed of several...
The Issue: The reason for this recall is Healgen Scientific Ltd. has determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 Recalled by PHILIPS...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Recalled by...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.