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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2606126080 of 48,376 recalls

Medical DeviceFebruary 15, 2018· Philips Medical Systems (Cleveland) Inc

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.

Class II — Potential Health HazardOngoing
FoodFebruary 15, 2018· Seggiano Usa Inc.

Recalled Item: Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g Recalled by...

The Issue: The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce &...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 15, 2018· Medline Industries Inc

Recalled Item: PVP Scrub Solution Recalled by Medline Industries Inc Due to Subpotent Drug:...

The Issue: Subpotent Drug: product not meeting the iodine assay level requirements...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2018· Fagron, Inc

Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...

The Issue: Microbial contamination of Non-Sterile Product; product contamination with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Avant-garde 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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Expression 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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS HI Recalled by Siemens Medical Solutions USA, Inc Due to Control...

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Impression 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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Stanbio Laboratory, LP

Recalled Item: RaPET¿ RF Latex Reagent used as a component in the Recalled by Stanbio...

The Issue: All patient serum samples yield a weakly positive test result.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Becton Dickinson & Company

Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold...

The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Pentax of America Inc

Recalled Item: Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled:...

The Issue: The duodenoscopes are being recalled in order to replace the forceps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Becton Dickinson & Company

Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold...

The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2018· Hetero Labs Limited Unit V

Recalled Item: Valacyclovir Tablets USP 1 gram Recalled by Hetero Labs Limited Unit V Due...

The Issue: Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2018· Nostrum Laboratories Inc

Recalled Item: Calcium Acetate Capsules Recalled by Nostrum Laboratories Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2018· Hetero Labs Limited Unit V

Recalled Item: Valganciclovir Tablets Recalled by Hetero Labs Limited Unit V Due to...

The Issue: Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2018· Arjohuntleigh Magog

Recalled Item: Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling Recalled by...

The Issue: The spreader bar can detach from the scale attachment under certain conditions.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2018· Arjohuntleigh Magog

Recalled Item: Quick Connect 272 KG Scale used with Maxi Sky 2 Recalled by Arjohuntleigh...

The Issue: The spreader bar can detach from the scale attachment under certain conditions.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Pentoxifylline USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund