Nevada recalls
3802 federal recalls on file affecting Nevada - 425 Nevada-specific plus 3377 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Azurion 5 M12 X-ray system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using Philips Azurion 7 M20 foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Azurion 7 M12 X-ray system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using Philips Azurion 7 B20 foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideContact Philips about your Azurion 7 B12 system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Azurion 3 M15 foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Azurion 3 M12 X-ray system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Allura Xper OR table foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideContact Philips about your Allura Xper X-ray system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Allura Xper FD20/20 OR Table
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Allura Xper FD20/20 X-ray system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips Allura Xper X-ray system
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideContact Philips about your ALLURA Xper FD10 table
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using Philips ALLURA Xper FD20 foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using affected Philips ALLURA X-ray tables
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using affected Philips ALLURA X-ray systems
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using affected Philips X-ray foot switches
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips ALLURA Xper system serial number
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideStop using Philips ALLURA Xper FD10 foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideCheck your Philips ALLURA X-ray foot switch
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DevicePhilipsClass IINationwideContact Philips about Allura Xper FD10C foot switch issue
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
- 2026-04-08FDA-DeviceSiemensClass IINationwideCheck Siemens Atellica CH A1c_E test results
A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate analyzers are not impacted by the recall. The frequency and magnitude of the negative bias and imprecision increase over time and are not consistent with the assay Instructions For Use (IFU). When this issue is present, Quality Control (QC) results demonstrate a negative trend and increased imprecision. The clinical impact of a negative (A1c_E) bias may lead to a delay in diagnosis for diabetes or lead to less-than-optimal treatment for existing diabetes.
- 2026-04-08FDA-DeviceReCor MedicalClass IINationwideDo not use ReCor Medical Paradise catheter
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
- 2026-04-08FDA-DeviceReCor MedicalClass IINationwideCheck Paradise renal denervation catheter lot M4907
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics ventilator settings
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics ventilator settings
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics ventilator settings
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DevicePhilipsClass INationwideCheck your Philips Respironics Trilogy Evo ventilator
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
- 2026-04-08FDA-DeviceAbiomedClass INationwideCheck your Impella Controller serial number
Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*) pumps.
- 2026-04-08FDA-DeviceAbiomedClass INationwideCheck your Abiomed Impella pump cassette
Increased risk of purge leaks with Generation 1 purge cassettes.
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