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. 1,106 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,106 in last 12 months

Showing 2781–2800 of 28,334 recalls

Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2024· St. Jude Medical

Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient...

The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2024· St. Jude Medical

Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial...

The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Recalled by Stryker...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil Recalled by...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CARROLLTON HIP FX Convenience kit used for surgical procedures Recalled by...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Stryker Corporation

Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch...

The Issue: There is a potential for the product to activate without manual input when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures Recalled by MEDLINE...

The Issue: Products within a Medline pack may be impacted by a packaging error in which...

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

Class II — Potential Health HazardOngoing