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. 2,525 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,525 in last 12 months

Showing 85018520 of 13,355 recalls

DrugOctober 19, 2016· Janssen Ortho L.L.C.

Recalled Item: Invokamet (canagliflozin and metformin HCl) tablets Recalled by Janssen...

The Issue: Labeling: Incorrect or Missing Package Insert - Xarelto prescribing...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2016· GSK Consumer Healthcare

Recalled Item: Zeasorb AF (miconazole nitrate) Recalled by GSK Consumer Healthcare Due to...

The Issue: Labeling Not Elsewhere Classified: front labels have the incorrect NDC or...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2016· Town and Country Compounding and Consultation Services, LLC

Recalled Item: HCG (Chorionic Gonadotropin Lyopholized) II Recalled by Town and Country...

The Issue: Subpotent Drug: due to failed potency results of 74% (spec. 80-125%).

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Olanzapine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: due to out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugOctober 12, 2016· Pharmedium Services, LLC

Recalled Item: Succinylcholine Chloride Recalled by Pharmedium Services, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: A portion of the batch quantity was...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets Recalled by Boehringer Ingelheim...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2016· Par Pharmaceutical, Inc.

Recalled Item: Travoprost Ophthalmic Solution USP Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Lack of Assurance of Sterility; damage to the internal portion of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2016· West-Ward Pharmaceutical

Recalled Item: PredniSONE Tablets USP Recalled by West-Ward Pharmaceutical Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Phenobarbital Tablets Recalled by West-Ward Pharmaceuticals Corp. Due to...

The Issue: Failed Dissolution Specifications: Phenobarbital Tablets have an out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2016· Amerisource Health Services

Recalled Item: Paricalcitol Capsules Recalled by Amerisource Health Services Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: This repackaged product was...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Range Trauma Kit Hardcase - Product Code 85-0889 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Range Trauma Kit ORG - Product Code 80-0213 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: USCG Boat Response Kit - Product Code 80-0353 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Aid Backpack Kit - Product Code 85-0917 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Mini Resupply Trauma Kit - Product Code 85-0835 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund