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. 2,039 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,039 in last 12 months

Showing 69016920 of 28,334 recalls

Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...

The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2023· BioFire Diagnostics, LLC

Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - Recalled by BioFire...

The Issue: Due to temperature excursions with products (products being stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carestream Health, Inc.

Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...

The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Carefusion 2200 Inc

Recalled Item: CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog...

The Issue: Product did not meet shelf-life testing requirements resulting in a breach...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· DiaSorin Molecular LLC

Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...

The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...

The Issue: Siemens Healthineers has received customer complaints and confirmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2023· Maquet Cardiovascular, LLC

Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...

The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides (concentrated)-In vitro diagnostic use in the...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Triglycerides_2: in vitro diagnostic use in the quantitative...

The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· Beckman Coulter, Inc.

Recalled Item: Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N)...

The Issue: An increased incidence of damage to the nut band from a new vendor (Boamax)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· CooperVision, Inc.

Recalled Item: Biofinity XR Toric 6-pack- Soft (hydrophilic) Contact Lens (extended wear)...

The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 26, 2023· CooperVision, Inc.

Recalled Item: Biofinity XR Toric Single Diagnostic lens- Soft (hydrophilic) Contact Lens...

The Issue: Manufactured with misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator PKG Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is the potential for patient desaturation events to occur under...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 25, 2023· Church & Dwight Inc

Recalled Item: Easy Read App associated with First Response Pregnancy Test Sticks Recalled...

The Issue: Church & Dwight First Response Pregnancy Kits was marketed with the Easy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Covidien, LP

Recalled Item: Tri-Staple 2.0 Black Intelligent Reload Recalled by Covidien, LP Due to...

The Issue: Affected lots have the potential for a broken sled vane, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2023· Stryker Corporation

Recalled Item: Triton Canister Software Catalog Number: GAUS-2. Intended adjunct in the...

The Issue: Triton Canister Software, Insert & Scanning Label may cause the Triton...

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

Class II — Potential Health HazardOngoing