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Surgical Instruments

πŸ₯ Medical Devices β€’ 7,015 recalls

An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the potential to lead to unintended delivery of medication when the pump module is not in running status or can result in faster than expected drug delivery flow when the pump is infusing.

May 6, 2019 Surgical Instruments Nationwide View Details β†’

The product may not have met sterility requirements . Use of a non-sterile device on a patient may expose the patient to infectious agents.

Jan 28, 2019 Surgical Instruments Nationwide View Details β†’

Potential for reporting low assay results

May 10, 2019 Surgical Instruments Nationwide View Details β†’

The sterile package seal for the Epi-Sense Guided Coagulation System may be compromised, and has a worst-case reasonable harm of infection if used.

May 29, 2019 Surgical Instruments Nationwide View Details β†’