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 38013820 of 50,223 recalls

DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2024· Viatris Inc

Recalled Item: Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent...

The Issue: Superpotent Drug and Subpotent Drug: potency failures obtained

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 18, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT Recalled by...

The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) Port Access Kit Recalled by MEDLINE...

The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT...

The Issue: Certain Medline kits were manufactured and distributed with Procedure Masks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 850 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 6 Plus Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2024· GE Medical Systems, LLC

Recalled Item: Tec 820 SEV Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...

The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 16, 2024· Grimmway Enterprises, Inc. dba Grimmway Farms

Recalled Item: --- Organic Baby Carrots --- Organic Baby Carrots 25 Grimmway Farms Recalled...

The Issue: Potential contamination with E. coli O121:H19

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2024· Grimmway Enterprises, Inc. dba Grimmway Farms

Recalled Item: --- Organic Whole Carrots --- Organic Carrot 125/6 Cal-Organic Farms...

The Issue: Potential contamination with E. coli O121:H19

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 16, 2024· Grimmway Enterprises, Inc. dba Grimmway Farms

Recalled Item: --- Organic Whole Carrots --- Organic Clip Carrots 50 Lbs Cal-Organic Farm...

The Issue: Potential contamination with E. coli O121:H19

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund