Class IIOngoingZ-0984-2025
Medtronic Perfusion Systems recalls DLP Pediatric One-Piece Arterial Cannulae
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Medtronic Perfusion Sy…MNJan 29, 2025
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–15 of 15 recalls
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
A possible sterility issue was detected in Coloplast's facility on some Coloplast products.
A possible sterility issue was detected in Coloplast's facility on some Coloplast products.