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 74817500 of 13,472 recalls

DrugNovember 30, 2017· Intrathecal Compounding Specialist, LLC

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

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 Fentanyl...

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 29, 2017· Blue Fusion Natural

Recalled Item: BLUE PEARL capsules Recalled by Blue Fusion Natural Due to Undeclared Sildenafil

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 I — Serious Health HazardOngoing
Refund
DrugNovember 29, 2017· Prinston Pharmaceutical Inc

Recalled Item: Valsartan Tablets Recalled by Prinston Pharmaceutical Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: confirmed customer complaint of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 28, 2017· EAI-JR286 INC

Recalled Item: Vertra Elemental Resistance (Octyl Methoxycinnamate 6% Recalled by EAI-JR286...

The Issue: CGMP Deviations: products manufactured in a manner that may impact product...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 28, 2017· Teva Pharmaceuticals USA

Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...

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

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

Class III — Low RiskOngoing
Refund
DrugNovember 21, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine Tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2017· Teva Pharmaceuticals USA

Recalled Item: Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Teva...

The Issue: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 5 Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 20 Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 500 iu Orally Disintegrating Tablets (ODT)...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Chloramphenicol 500 mg Sulfamethoxazole 500 mg Amphotericin 50 mg Otic...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Trimix #23F (Prostaglandin E1 6 mcg/ Papaverine HCl 17.8 mg/ Recalled by KRS...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin 500 mcg Orally Disintegrating Tablets (ODT) Recalled by KRS...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Benzocaine 20% Recalled by KRS Global Biotechnology, Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: T-105 (Prostaglandin E1 Recalled by KRS Global Biotechnology, Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Chloramphenicol 500 mg Amphotericin 50 mg Otic Powder packaged in jars...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: 7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule Recalled by KRS...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Anastrozole SR 1 mg Capsules Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund