State

Nevada product recalls

73,106 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total: 5,696
Critical: 951
Severe: 1,479
Most recent: 2026-09-25

Of the 5,696 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,479 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11501–11525 of 78802

HighFDA (Devices)·Z-2022-2024·2024-06-12
GlideScope Core 15-inch Monitor Software Issue Causes Potential Image Loss
Verathon recalls 1,706 GlideScope Core 15-inch FHD monitors due to a software defect in versions v1.7 and earlier. The defect can cause loss or degradation of image when the monitor is used with other connectable devices.
Product
Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description: Serialized Monitor
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-2011-2024·2024-06-12
Vascular Graft Component Separation Risk Triggers Worldwide Device Recall
Atrium Medical recalls FLIXENE vascular grafts due to reported separation of the Swivel Rod from the Swivel Core, creating gaps that could affect device function. Over 53,000 units worldwide are affected.
Product
FLIXENE, 6X30, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2005-2024·2024-06-12
FLIXENE Vascular Graft Recalled for Slider Swivel Rod Separation
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reports of the slider swivel rod separating from the swivel core. The separation could affect device function during vascular procedures.
Product
FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1977-2024·2024-06-12
Vascular graft slider component separation reported in ADVANTA VXT
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to separation of the Slider GDS Swivel Rod from the Swivel Core. Over 53,000 units affected worldwide.
Product
ADVANTA VXT, 6X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2006-2024·2024-06-12
Vascular graft component separation reported in FLIXENE Slider GDS devices
Atrium Medical Corporation is recalling FLIXENE vascular grafts due to reported separation between the Slider GDS Swivel Rod and Swivel Core, affecting 53,308 units distributed worldwide.
Product
FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0534-2024·2024-06-12
Prescription migraine drug recalled for manufacturing impurity above FDA limit
Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate tablets for exceeding FDA acceptable limits of N-Nitroso Desmethyl Rizatriptan impurity. The recall affects 2,400 cartons distributed nationwide.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1936-2024·2024-06-12
Medline Syringes Recalled Due to Leaks, Breakage, and Quality Issues
Medline Industries is recalling over 2.3 million syringes due to identified leaks, breakage, and quality issues that may pose risks to patient health. The affected syringes were distributed nationwide and internationally.
Product
Syringes labeled as: a) SYR 10ML L/L CONTROL, Item Numbers: 1. DNSC91881, 2. DYNJSYRPPC10; b) SYRINGE 20ML BLUE L/L LOW PR, Item Number: DYNJSYRPP20B; c) SYRINGE 20ML RED L/L LOW PRESS, Item Number: DYNJSYRPP20R; d) SYRINGE 10ML RED L/L LOW PR, Item Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1990-2024·2024-06-12
Vascular graft separation issue prompts FDA recall of Atrium Medical ADVANTA VXT units
Atrium Medical Corporation is recalling its ADVANTA VXT vascular grafts due to complaints of swivel rod separation from the swivel core, which could affect device function and patient safety.
Product
ADVANTA VXT, 8X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1984-2024·2024-06-12
Vascular graft separation reported in ADVANTA VXT medical devices
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Approximately 53,308 units have been affected worldwide.
Product
ADVANTA VXT, 7X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1978-2024·2024-06-12
ADVANTA VXT Vascular Graft Recalled for Component Separation
ADVANTA VXT vascular grafts are recalled due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between components.
Product
ADVANTA VXT, 7X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1996-2024·2024-06-12
ADVANTA VXT Vascular Grafts Recalled for Slider Component Separation Risk
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Approximately 53,308 units worldwide are affected.
Product
ADVANTA VXT, 4-7X70, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2028-2024·2024-06-12
Philips Tempus LS-Manual Defibrillator may malfunction from electrical interference
Simultaneous ECG measurements with multiple devices can cause electrical interference that may prevent this defibrillator from functioning properly. The recall affects 1,745 units distributed nationwide.
Product
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1945-2024·2024-06-12
Proton Therapy System May Continue Irradiation When Accelerator Control Parameters Out of Tolerance
Ion Beam Applications' IBA Proton Therapy System PROTEUS 235 may continue delivering radiation when critical accelerator control parameters are outside defined tolerances. Affected users should contact the manufacturer regarding firmware updates.
Product
IBA Proton Therapy System - PROTEUS 235 - Designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1985-2024·2024-06-12
Vascular Graft Swivel Rod Separation Recalled Due to Component Failure
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of separation between the Slider GDS Swivel Rod and Swivel Core, which could affect device function.
Product
ADVANTA VXT, 8X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1997-2024·2024-06-12
Vascular Graft Component Separation in ADVANTA VXT Medical Devices
ADVANTA VXT vascular grafts are being recalled because the Slider GDS Swivel Rod may separate from the Swivel Core. This affects about 53,308 units distributed worldwide including the US.
Product
ADVANTA VXT, 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1994-2024·2024-06-12
Vascular graft recalled due to slider component separation risk
Atrium Medical's ADVANTA VXT vascular grafts are being recalled worldwide due to reports of the Slider GDS Swivel Rod separating from the Swivel Core. The separation creates a gap that could compromise device function.
Product
ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1948-2024·2024-06-12
HA FlexTrak Patient Transport Device Oil Leak Poses Slipping Hazard
Oil may leak from the HA FlexTrak patient transport device when the hydraulic pedal is pressed, creating a potential slipping or falling hazard on the floor.
Product
HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006411
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1957-2024·2024-06-12
Vascular graft recalled due to slider component separation risk
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reports of the slider GDS swivel rod separating from the swivel core. Approximately 53,308 units are affected worldwide.
Product
ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0533-2024·2024-06-12
Rizatriptan Benzoate Tablets Recalled for Excessive N-Nitroso Impurity
Glenmark Pharmaceuticals recalls certain Rizatriptan Benzoate tablets due to N-Nitroso Desmethyl Rizatriptan impurity levels exceeding FDA acceptable limits. The affected lots were distributed nationwide.
Product
RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1940-2024·2024-06-12
Synchro SELECT Guidewires may have PTFE coating damage
Stryker Neurovascular recalls certain lots of Synchro SELECT Guidewires due to PTFE coating damage that may occur when using a backloading technique. The damage is caused by sharper-than-intended edges on older introducer versions.
Product
The Synchro SELECT Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014in. The guidewires are compatible with existing microcatheters used in common procedures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1970-2024·2024-06-12
Vascular graft recalled for slider rod component separation
Atrium Medical is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from its Swivel Core. The recall affects 53,308 units distributed worldwide.
Product
ADVANTA VXT, 8X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1973-2024·2024-06-12
Atrium ADVANTA VXT Vascular Graft Slider Rod Separation
ADVANTA VXT vascular grafts may have separation of the Slider GDS Swivel Rod from the Swivel Core. Atrium is recalling affected units.
Product
ADVANTA VXT, 6X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1967-2024·2024-06-12
ADVANTA VXT vascular graft slider component separation recall
ADVANTA VXT vascular grafts may experience separation of the slider component from its core. This Class II recall affects 53,308 units distributed worldwide.
Product
ADVANTA VXT, 8X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1963-2024·2024-06-12
Atrium Medical Vascular Graft Swivel Component Separation Recall
Atrium Medical recalled 53,308 ADVANTA VXT vascular grafts worldwide due to reported separation of the swivel rod from the swivel core. The affected units were distributed throughout the United States and to 60 additional countries.
Product
ADVANTA VXT, 6X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2025-2024·2024-06-12
Bedside Monitor Software Issue Causes False Oxygen Saturation Probe Failure Alarms
Nihon Kohden's BSM-3000 Series Bedside Monitors may produce false SpO2 probe failure alarms due to a software issue. Healthcare facilities should contact the manufacturer for guidance.
Product
BSM-3000 Series Bedside Monitor REF BSM-3572A The Life Scope BSM-3000 Series Bedside Monitoring System is intended to monitor, display and record physiological data to provide cardiac and vital signs monitoring within a medical facility.
Category
Medical Device
Distribution
Distributed nationwide