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 74617480 of 13,472 recalls

DrugDecember 14, 2017· Teva Pharmaceuticals USA

Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...

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

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 13, 2017· ALLERGAN

Recalled Item: INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL)...

The Issue: Failed Stability Specifications: Product stability testing results did not...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2017· Keryx Biopharmaceuticals, Inc.

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Keryx Biopharmaceuticals, Inc....

The Issue: Presence of Foreign Substance: Reports have been received of damaged...

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

Class III — Low RiskOngoing
Refund
DrugDecember 7, 2017· SCA Pharmaceuticals

Recalled Item: Ephedrine sulfate 5 mg/mL in 0.9% Sodium Chloride 10 mL in Single Dose...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - product label was...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena deep clean purifying whipped foam cleanser Recalled by Johnson &...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· BotanicalNow

Recalled Item: BodySlim Herbal Advanced technology & Strong formula capsules Recalled by...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Elevated 4-Holiday Trays (contains Neutrogena Deep Clean...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2017· Johnson & Johnson

Recalled Item: Neutrogena Acne Proofing whipped foam cleanser Recalled by Johnson & Johnson...

The Issue: Defective Container: products showed leakage (bubbles, foaming) of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2017· AuroMedics Pharma LLC

Recalled Item: Pantoprazole Sodium for Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2017· ALLERGAN

Recalled Item: Viokace (pancrelipase) tablets Recalled by ALLERGAN Due to Subpotent Drug:...

The Issue: Subpotent Drug: One lot of Viokace is being recalled since product stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

Recalled Item: All sterile drug preparations remaining within expiry prepared from...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

Recalled Item: All sterile drug preparations remaining within expiry prepared from...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2017· BYL Solutions Inc.

Recalled Item: Bull Capsules Recalled by BYL Solutions Inc. Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA; product found to be tainted with...

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

Class III — Low RiskOngoing
Refund