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. 1,790 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,790 in last 12 months

Showing 2668126700 of 48,376 recalls

DrugNovember 21, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2017· Teva Pharmaceuticals USA

Recalled Item: Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Teva...

The Issue: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine Tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...

The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...

The Issue: When calculating electron Monte Carlo dose with a very large number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2017· Edan Diagnostics

Recalled Item: EDAN Telemetry Transmitter Recalled by Edan Diagnostics Due to Firm became...

The Issue: Firm became aware that it distributed 7 units in the U.S. that included a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2017· CareFusion 303, Inc.

Recalled Item: Alaris Syringe Pump Recalled by CareFusion 303, Inc. Due to The syringe...

The Issue: The syringe plunger grippers may fail to automatically close around the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PCA Pump Recalled by CareFusion 303, Inc. Due to The syringe plunger...

The Issue: The syringe plunger grippers may fail to automatically close around the...

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

Class II — Potential Health HazardOngoing
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 20 Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 500 iu Orally Disintegrating Tablets (ODT)...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Chloramphenicol 500 mg Amphotericin 50 mg Otic Powder packaged in jars...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Anastrozole SR 1 mg Capsules Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Hydroxocobalamin 1 mg/mL 30 mL Vial For IM Use Recalled by KRS Global...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Acetate 3 mg/ GHRP6 3 mg Recalled by KRS Global Biotechnology,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Liothyronine SR (T3) 20 mcg Capsule Recalled by KRS Global Biotechnology,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Anastrozole 0.5 mg Capsules Recalled by KRS Global Biotechnology, Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Vitamin 9 A/B Lyophilized Vial Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 6 Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund