Alabama recalls

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Due to increased complaints for broken/frayed grip cables for reusable instruments.

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.

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.

There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.

Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.

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.

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.

Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.

Surgical light assembly may not adequate support the weight of the ceiling cover.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.