Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 685–696 of 801 recalls
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket.…
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.