Medtronic DLP Retrograde Cardioplegia Cannulae

Product Medtronic DLP Retrograde Cardioplegia Cannulae Issue Medical devices - Sterility What to do Contact the manufacturer if you require additional information. Audience Healthcare

On 8-January-2026, Medtronic received a complaint from the U.S. reporting that a seal of a pouch containing the cannula was not fully sealed (chevron side) and opened to the air. The customer reported that they identified seventeen (17) cannulae with open pouches and therefore considered the product unsterile. There was no patient involvement in the complaint.

RA-82009