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 76617680 of 13,472 recalls

DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Pediatric IV Kit. Packaged in USA for Medline Industries Recalled by...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Aplicare Povidone-Iodine Prep Pad Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Concordia Trunk Kit. Packaged for Medline Industries Recalled by...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Incision and Drainage Tray Kit Recalled by Medline Industries Inc...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Hip Replacement Recalled by Medline Industries Inc Due to Subpotent...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Gel USP Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: traces of Dapsone were found in the...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Baxter Healthcare Corporation

Recalled Item: Intralipid 20% Recalled by Baxter Healthcare Corporation Due to Temperature...

The Issue: Temperature Abuse: A portion of this product lot was exposed to subfreezing...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: RHINO 7 Platinum 5000 Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 14, 2017· Medisca, Inc.

Recalled Item: Aminocaproic Acid Recalled by Medisca, Inc. Due to CGMP Deviations: Product...

The Issue: CGMP Deviations: Product manufactured for Industrial Use but was labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2017· Amgen, Inc.

Recalled Item: Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of...

The Issue: Presence of particulate matter: glass flakes identified as lamellae observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2017· Vi-Jon, Inc.

Recalled Item: Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 Recalled by...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
DrugSeptember 5, 2017· Teva Pharmaceuticals USA

Recalled Item: Acarbose Tablets Recalled by Teva Pharmaceuticals USA Due to Labeling:...

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

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2017· Aidarex Pharmaceuticals LLC

Recalled Item: Phentermine Recalled by Aidarex Pharmaceuticals LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specification; out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 5, 2017· Genentech, Inc.

Recalled Item: Activase (alteplase) Recalled by Genentech, Inc. Due to...

The Issue: Non-Sterility:presence of cracked or chipped glass at the neck of Sterile...

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

Class I — Serious Health HazardOngoing
Refund