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. 2,702 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,702 in last 12 months

Showing 45014520 of 13,472 recalls

DrugJune 18, 2020· MICHIGAN HERBAL REMEDIES

Recalled Item: Tasty Drops Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead

The Issue: Chemical contamination: product contains elevated levels of undeclared lead.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 18, 2020· MICHIGAN HERBAL REMEDIES

Recalled Item: Herbzeedy Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead

The Issue: Chemical contamination: product contains elevated levels of undeclared lead.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 18, 2020· MICHIGAN HERBAL REMEDIES

Recalled Item: Made by Hemp 1000MG Hemp Extract Recalled by MICHIGAN HERBAL REMEDIES Due to...

The Issue: Chemical contamination: product contains elevated levels of undeclared lead.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 18, 2020· MICHIGAN HERBAL REMEDIES

Recalled Item: Recovery Releaf Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead

The Issue: Chemical contamination: product contains elevated levels of undeclared lead.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 18, 2020· MICHIGAN HERBAL REMEDIES

Recalled Item: BC Hemp Co. Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead

The Issue: Chemical contamination: product contains elevated levels of undeclared lead.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 16, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Childrens Robitussin Honey Cough and Chest Congestion DM Recalled by...

The Issue: Defective Delivery System: the dosing cups are missing graduations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Childrens Dimetapp Cold & Cough Recalled by Glaxosmithkline Consumer...

The Issue: Defective Delivery System: the dosing cups are missing graduations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 13, 2020· Yusef Manufacturing Laboratories, LLC

Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...

The Issue: Superpotent Drug: The beginning portion of the batch appears to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Clozapine Tablets USP tablet Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· The Harvard Drug Group

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...

The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Defective Container: Customer complaints received of a crimp defect while...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Defective Container: Customer complaints received of a crimp defect while...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· American Health Packaging

Recalled Item: Nabumetone Tablets Recalled by American Health Packaging Due to Labeling Not...

The Issue: Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with...

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

Class III — Low RiskOngoing
Refund
DrugJune 10, 2020· Crown Laboratories

Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· Crown Laboratories

Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· Alembic Pharmaceuticals Limited

Recalled Item: Aripiprazole Tablets Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2020· Marksans Pharma Limited

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

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund