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. 2,706 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,706 in last 12 months

Showing 42814300 of 13,472 recalls

DrugOctober 8, 2020· Denton Pharma, Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Denton Pharma,...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2020· Baxter Healthcare Corporation

Recalled Item: Bupivacaine Hydrochloride in 8.25% Dextrose Injection Recalled by Baxter...

The Issue: Presence of particulate matter in solution - black and transparent particles

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Candesartan Cilexetil and Hydrochlorothiazide Tablets Recalled by Mylan...

The Issue: Out-of-specification organic impurity results obtained during routine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2020· Marksans Pharma Limited

Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2020· Teligent Pharma, Inc.

Recalled Item: Fluocinonide Ointment USP 0.05% Recalled by Teligent Pharma, Inc. Due to...

The Issue: Failed Impurities/Degradation - Out-of-specification results for...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Happy Ducts Compress Recalled by Wishgarden Herbs, Incorporated Due to...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· VistaPharm, Inc.

Recalled Item: NYSTATIN ORAL SUSPENSION Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurties/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Cord Care POWDER Recalled by Wishgarden Herbs, Incorporated Due to Microbial...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2020· Wishgarden Herbs, Incorporated

Recalled Item: Goldenseal POWDER Recalled by Wishgarden Herbs, Incorporated Due to...

The Issue: Microbial Contamination of a Non-Sterile Product: Product tested positive...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 23, 2020· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: RIOMET ER (metformin hydrochloride for extended-release oral suspension)...

The Issue: CGMP Deviations: Detection of N-nitrosodimethylamine (NDMA) impurity in...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 16, 2020· Perrigo Company PLC

Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2020· Arbor Pharmaceuticals Inc.

Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund