Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR
Certain lots of product have the potential for a sterile barrier breach.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 24 recalls
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
Certain lots of product have the potential for a sterile barrier breach.
The catheters may not retain their shape.
The catheters may not retain their shape.
The catheters may not retain their shape.
Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay.…
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.