Nebraska recalls
3397 federal recalls on file affecting Nebraska - 322 Nebraska-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-28FDA-DeviceGVSClass IIStop using GVS SQ40S blood transfusion filters
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.
- 2026-01-28FDA-DevicePhilipsClass IINationwideCheck Philips Patient Information Center iX settings
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan iT20 telemetry transmitter
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck Edan iM8 patient monitor security
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan M3A vital signs monitor
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan M3B monitor for security update
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan fetal monitoring system
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck Edan MFM-CMS central monitoring system
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan patient monitor serial number
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan patient monitor model
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan iM20 patient monitor
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan patient monitor for updates
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan patient monitor for cybersecurity issues
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck Edan iM3s monitor serial number
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck Edan iM3 monitor for security update
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck Edan M3 vital signs monitors for security update
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan fetal monitor model
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceEdan DiagnosticsClass IINationwideCheck your Edan fetal monitor model and serial number
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
- 2026-01-28FDA-DeviceCommunity ProductsClass IINationwideCheck your Rifton E-Pacer gait trainer for fraying
Potential for fraying on the body support strap.
- 2026-01-28FDA-DeviceCommunity ProductsClass IINationwideCheck your Rifton TRAM lift device for strap damage
Potential for fraying on the body support strap.
- 2026-01-28FDA-DeviceCommunity ProductsClass IINationwideCheck your Rifton TRAM lift device
Potential for fraying on the body support strap.
- 2026-01-28FDA-DeviceSysmexClass IINationwideCheck your Sysmex TS-10/TS-10H Tube Sorter
Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift.
- 2026-01-28FDA-DeviceBeckman CoulterClass IINationwideStop using Beckman Coulter LDL Cholesterol OSR6x96
Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent showed clinically significant interference due to triglyceride concentration up to 1500 mg/dL may cause a maximum positive bias of up to 28.8% in low LDL Cholesterol samples (concentration 80 mg/dL) and up to 11.02% in high LDL Cholesterol samples (concentration 160mg/dL).
- 2026-01-28FDA-DeviceIntuitive SurgicalClass IINationwideCheck your Ion Vision Probe Bag lot number
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
- 2026-01-28FDA-DeviceTyber MedicalClass IINationwideCheck Tyber Medical VOLT wrist plates
The supplier manufactured anatomical left plates with an incorrect thread orientation.
- 2026-01-28FDA-DeviceTyber MedicalClass IINationwideCheck Tyber Medical VOLT wrist plates
The supplier manufactured anatomical left plates with an incorrect thread orientation.
- 2026-01-28FDA-DeviceLeaseir TechnologiesClass IINationwideCheck your Leaseir MHR Xcell laser console label
The console label for affected devices is missing the "DANGER" symbol.
- 2026-01-28FDA-DeviceMerit MedicalClass IINationwideStop using Merit Medical angioplasty packs
Inflation device handle may detach from the syringe during procedure.
- 2026-01-28FDA-DeviceMerit MedicalClass IINationwideStop using Merit Medical Custom Procedure Kits
Inflation device handle may detach from the syringe during procedure.
- 2026-01-28FDA-DeviceMerit MedicalClass IINationwideStop using Merit Medical Custom Manifold Kit
Inflation device handle may detach from the syringe during procedure.
Get notified about new Nebraska recalls
Free weekly digest. Add Nebraska to your profile to filter alerts to your state.
Get the Sunday Brief