Recalls — last 90 days
- 2026-04-08FDA-DeviceIntuitive Surgical, Inc.Class IIStop using recalled da Vinci scissors instruments
Due to increased complaints for broken/frayed grip cables for reusable instruments.
- 2026-04-08FDA-DeviceOlympus Corporation of the AmericasClass IIStop using affected Olympus SOLTIVE Pro laser units
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.
- 2026-04-08FDA-DeviceOlympus Corporation of the AmericasClass IIStop using affected Olympus SOLTIVE laser systems
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.
- 2026-04-08FDA-DeviceMedline Industries, LPClass IIStop using Medline radiology kits lot 25GBB924
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
- 2026-04-08FDA-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck your Philips Vue Motion V12 software
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
- 2026-04-08FDA-DeviceMedline Industries, LPClass IIStop using Medline ENFIT G-tube connector kits
Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.
- 2026-04-08FDA-DeviceMedline Industries, LPClass IIStop using Medline ENFIT G-tube connectors
Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.
- 2026-04-08FDA-DeviceUltradent Products, Inc.Class IIStop using Ultradent Jiffy polisher cups
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
- 2026-04-08FDA-DeviceStryker CommunicationsClass IICheck Stryker CHROMOPHARE surgical light ceiling support
Surgical light assembly may not adequate support the weight of the ceiling cover.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IIStop using Mentor Artoura tissue expanders
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IIStop using Mentor Artoura Breast Tissue Expanders
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IIStop using Mentor Artoura Breast Tissue Expanders
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IIStop using Mentor CPX 4 breast tissue expanders
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IIStop using Mentor CPX 4 tissue expanders
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IIStop using Mentor CPX 4 tissue expanders
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DeviceMentor Texas, LP.Class IICheck your Mentor CPX 4 tissue expander infusion set
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
- 2026-04-08FDA-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIStop using Philips Azurion 5 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIStop 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIStop 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIContact 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIContact 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IICheck 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-DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Class IIContact 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.