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 78817900 of 13,355 recalls

DrugJune 1, 2017· Lucid Pharma LLC

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid...

The Issue: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2017· L. Perrigo Company

Recalled Item: Option 2 Recalled by L. Perrigo Company Due to Defective Container: Carton...

The Issue: Defective Container: Carton is missing the tablet blister strip and tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...

The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2017· Teva Pharmaceuticals

Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...

The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2017· Mckesson Packaging Services

Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2017· AstraZeneca Pharmaceuticals, LP

Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...

The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...

The Issue: Presence of foreign substance: The recall was initiated due to black...

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

Class III — Low RiskOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 19, 2017· DYNAMIC TECHNICAL FORMULATIONS

Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules Recalled by DYNAMIC...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: HYDROmorphone HCL in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable Recalled by...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· Forest Laboratories, LLC

Recalled Item: Saphris 10 mg (asenapine) sublingual tablets Recalled by Forest...

The Issue: Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· Hospira Inc., A Pfizer Company

Recalled Item: Levophed norepinephrine bitartrate Recalled by Hospira Inc., A Pfizer...

The Issue: GMP Deviation; A foreign stopper was observed during packaging of a lot of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCL in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund