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. 2,702 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,702 in last 12 months

Showing 49014920 of 13,472 recalls

DrugNovember 25, 2019· Apothecus Pharmaceutical Corp.

Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....

The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2019· Medisca, Inc.

Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· OraLabs, Incorporated

Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...

The Issue: Cross contamination with other products: undeclared contaminants of phenol...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 25, 2019· AuroMedics Pharma LLC

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Product complaints of discoloration after reconstitution of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2019· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL Recalled by Pacira Pharmaceuticals, Inc. Due to Sub Potent Drug: Out...

The Issue: Sub Potent Drug: Out of Specification (OOS)

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· American Health Packaging

Recalled Item: Ranitidine Tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2019· AuroMedics Pharma LLC

Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...

The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Akorn, Inc.

Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...

The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2019· Grato Holdings, Inc.

Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...

The Issue: Labeling mix-up - Indications on product label are incorrect.

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

Class III — Low RiskOngoing
Refund