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 75817600 of 13,472 recalls

DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: fentaNYL citrate 1000 mcg (10 mcg/mL) 100 mL Cassette in 0.9% Sodium...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Norepinephrine Bitartrate16 mg added to 0.9% Sodium Chloride 250 mL bag...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· AVKARE Inc.

Recalled Item: Duloxetine Delayed-release Capsules USP Recalled by AVKARE Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: slightly elevated levels of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2017· Kiriko, LLC.

Recalled Item: A1 Slim Recalled by Kiriko, LLC. Due to Undeclared Sibutramine

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2017· Purdue Pharma, LP

Recalled Item: Betadine Solution Swabstick Povidone-Iodine Solution USP Recalled by Purdue...

The Issue: Subpotent Drug: The laminate used to make the pouches was reversed such that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Famotidine tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Famotodine has an out of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2017· Unichem Pharmaceuticals Usa Inc

Recalled Item: Bisoprolol Fumarate tablets Recalled by Unichem Pharmaceuticals Usa Inc Due...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2017· Leading Pharma, LLC

Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2017· United Pharmacy

Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...

The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· The Harvard Drug Group

Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2017· Sandoz Inc

Recalled Item: Ampicillin for Injection Recalled by Sandoz Inc Due to Labeling: Missing...

The Issue: Labeling: Missing Label: customer complaint that some vials of ampicillin...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension USP Recalled by Precision Dose Inc. Due to...

The Issue: Subpotent Drug: low out of specification results.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund