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. 2,722 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,722 in last 12 months

Showing 29612980 of 50,223 recalls

Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) LARGE BIOPSY PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PERI GYN PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: to RES Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to There is a...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) BASIC CATARACT...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PAIN PACK Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) INTUBATION TRAY...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) PRECIP TRAY...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Convenience kits used for various procedures: 1) DR. KHAN Recalled...

The Issue: There is a potential for open/weak seals on purchased breather pouches used...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe...

The Issue: During some clinical cases, it has been observed that the SO2 value may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter NovumIQ Syringe INFUSION SYSTEM Recalled by Baxter Healthcare...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2025· ZIMMER ORTHOPEDICS MANFACTURING LIMITED-GALWAY

Recalled Item: Comprehensive Shoulder Stem Recalled by ZIMMER ORTHOPEDICS MANFACTURING...

The Issue: Five complaints received where surgeon was unable to remove and/or connect...

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

Class II — Potential Health HazardOngoing
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 25 mg Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 12.5 mg Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets USP 6.25 mg Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund