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 9811000 of 50,223 recalls

DrugOctober 20, 2025· Golden State Medical Supply Inc.

Recalled Item: NIACIN Extended-Release Tablets Recalled by Golden State Medical Supply Inc....

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2025· Imprimis NJOF, LLC

Recalled Item: Klarity-C Drops (Cyclosporine) 0.1% Recalled by Imprimis NJOF, LLC Due to...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 20, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System....

The Issue: Potential for anesthesia leakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System....

The Issue: Potential for anesthesia leakage.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2025· Medtronic Perfusion Systems

Recalled Item: Medtronic HR-ACT (High Range Activated Clotting Time Cartridges) Recalled by...

The Issue: Medtronic personnel observed trace amounts of dry blood on the external...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2025· Auris Health, Inc

Recalled Item: MONARCH Bronchoscope. Model Number: MBR-000211-B Recalled by Auris Health,...

The Issue: Potential that product was leak tested with equipment outside of its...

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

Class II — Potential Health HazardOngoing
FoodOctober 17, 2025· Town Food Service Equip Co Inc

Recalled Item: Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1QT Recalled by...

The Issue: Product found to contain leachable lead levels.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2025· Aero Healthcare

Recalled Item: Acetaminophen 500mg Caffeine 65mg caplets Recalled by Aero Healthcare Due to...

The Issue: Labeling: Label Mix-up. This issue affects the outer box labeling only. The...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 17, 2025· Straumann USA LLC

Recalled Item: Emdogain Recalled by Straumann USA LLC Due to The possibility for this...

The Issue: The possibility for this product that is intended for demonstration purposes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· INTELERAD MEDICAL SYSTEMS INCORPORATED

Recalled Item: IntelePACS - InteleConnect / TechPortal Recalled by INTELERAD MEDICAL...

The Issue: Software application that receives digital images and data to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris infusion Pump Module 8100 Recalled by CareFusion 303, Inc. Due to...

The Issue: If infusion pump is dropped or severely jarred this may damage the pump...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2025· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an Recalled...

The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· TECHNO-PATH MANUFACTURING LTD.

Recalled Item: Multichem ID-B. Model Number: SR103B. Intended for use as an Recalled by...

The Issue: Potential of negative recovery of the HBsAg analyte across two (2) lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2025· Mozarc Medical US LLC

Recalled Item: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions...

The Issue: A potential issue with the seal integrity of header bag packaging.

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

Class II — Potential Health HazardOngoing
FoodOctober 16, 2025· M.C.I. Foods, Inc.

Recalled Item: Egg and Cheese Breakfast Burrito Recalled by M.C.I. Foods, Inc. Due to...

The Issue: Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria...

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

Class I — Serious Health HazardOngoing
Refund