Applied Medical Resources Corp recalls Kii Low Profile
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–6 of 6 recalls
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Due to complaints their is the potential that irrigation solution may leaked into the handpiece and battery pack causing it to malfunction.