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Medtronic Perfusion Systems recalls DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Recalled January 29, 2025 · FDA recall Z-0984-2025 · Medtronic Perfusion Systems
Hazard
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae. · FDA Class II
Units
745 units
Sold at
Worldwide - US Nationwide distribution.
Description
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Product
DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →