Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,684 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,684 in last 12 months

Showing 79417960 of 13,472 recalls

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: 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 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 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· 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· 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
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: morphine sulfate 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: MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable Recalled...

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: ceFAZolin sodium added to 100 mL 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· 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· 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: fentaNYL (as citrate) 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