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. 2,521 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,521 in last 12 months

Showing 97419760 of 48,376 recalls

DrugFebruary 6, 2023· Alvogen, Inc

Recalled Item: Levothyroxine Sodium Tablets Recalled by Alvogen, Inc Due to Sub-Potent...

The Issue: Sub-Potent Drug: Out of specification for assay at the 24 month interval.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2023· Securitas Healthcare LLC

Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...

The Issue: The mobile application for Android devices downloaded from the Google Play...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2023· Biomerieux Inc

Recalled Item: MYLA comprises AST Filters in conjunction with VITEK MS Recalled by...

The Issue: For users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as...

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

Class II — Potential Health HazardOngoing
DrugFebruary 3, 2023· Leadiant Biosciences, Inc.

Recalled Item: Abelcet (Amphotericin B Lipid Complex) Injection Recalled by Leadiant...

The Issue: Lack of assurance of sterility: Medial fill with presence of Cupriavidus...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 3, 2023· KEURIG DR PEPPER

Recalled Item: Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods Recalled...

The Issue: Product contains black tea, resulting in caffeine being undeclared.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2023· Avanos Medical, Inc.

Recalled Item: Avanos Ballard Oral Care Swab Recalled by Avanos Medical, Inc. Due to...

The Issue: Incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2023· Instrumentation Laboratory

Recalled Item: ACL ELITE designed specifically for clinical use in the Recalled by...

The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2023· Instrumentation Laboratory

Recalled Item: ACL ELITE PRO-Analyzer designed specifically for clinical use in the...

The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2023· Instrumentation Laboratory

Recalled Item: ACL ELITE- Analyzer designed specifically for clinical use in the Recalled...

The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2023· Instrumentation Laboratory

Recalled Item: ACL ELITE PRO )-Analyzer designed specifically for clinical use in Recalled...

The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2023· Avanos Medical, Inc.

Recalled Item: BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...

The Issue: Potential for product manifold to crack during use on patients, possibly...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2023· Avanos Medical, Inc.

Recalled Item: BALLARD ACCESS Closed Suction System for Neonates/Pediatrics Recalled by...

The Issue: Potential for product manifold to crack during use on patients, possibly...

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

Class I — Serious Health HazardOngoing
DrugFebruary 2, 2023· Advantice Health, Llc

Recalled Item: Dermoplast FIRST AID ANTIBACTERIAL SPRAY (Benzethonium chloride 0.2% First...

The Issue: Subpotent Drug: Low assay observed in one of the two active ingredients...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 2, 2023· Navada Imports

Recalled Item: Sunflower Lecithin Liquid Packaged in 2 Recalled by Navada Imports Due to...

The Issue: Undeclared peanut allergen

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

Class III — Low RiskOngoing
Refund
FoodFebruary 2, 2023· Navada Imports

Recalled Item: Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes Recalled...

The Issue: Undeclared peanut allergen

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

Class III — Low RiskOngoing
Refund
FoodFebruary 2, 2023· Navada Imports

Recalled Item: Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes Recalled by...

The Issue: Undeclared peanut allergen

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

Class III — Low RiskOngoing
Refund
FoodFebruary 2, 2023· Navada Imports

Recalled Item: Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes Recalled by Navada...

The Issue: Undeclared peanut allergen

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 2, 2023· Miach Orthopaedics

Recalled Item: BEAR Implant (Bridge-Enhanced ACL Restoration) Recalled by Miach...

The Issue: The field action was initiated in February of 2023 and was limited to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET...

The Issue: If, during the procedure, X-ray has been released and a image has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2023· Boston Scientific Corporation

Recalled Item: Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A...

The Issue: Cease use of the Habib EndoHPB Bipolar RF Catheter with the ERBE VIO3...

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

Class II — Potential Health HazardOngoing