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. 1,070 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,070 in last 12 months

Showing 14101–14120 of 50,223 recalls

DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Relief Allergy Relief D Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Midazolam in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: 12 HR Allergy & Congestion Relief Fexofenadine HCl Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2...

The Issue: (1)Start-up problem: Intermittently at start-up of the system, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B...

The Issue: Due to a calculation error in the measurement when using 2D trace (manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: BV Endura with Software Release 2.3- A mobile Recalled by Philips North...

The Issue: Instructions for Use do not specify the maximum surface temperature of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: Veradius Unity with Software Release 2.1- Amobile Recalled by Philips North...

The Issue: Instructions for Use do not specify the maximum surface temperature of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: BV Pulsera with Software Release 2.3-A mobile Recalled by Philips North...

The Issue: Instructions for Use do not specify the maximum surface temperature of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Acclarent, Inc.

Recalled Item: TruDi NAV Suction Instruments: 0-Degree Recalled by Acclarent, Inc. Due to...

The Issue: Suction Instruments were incorrectly calibrated so they may not meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2021· Orchestrate Orthodontic Technologies, Inc.

Recalled Item: O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing...

The Issue: Due to product label/labeling being altered from it's approved state.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2021· Medtronic Navigation, Inc.

Recalled Item: Stealthstation System w/ Stealthstation Cranial Software 3.1.1 Recalled by...

The Issue: Cranial biopsy procedure software can enter a state where the biopsy depth...

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

Class I — Serious Health HazardOngoing