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🇨🇦 Medtronic DLP Retrograde Cardioplegia Cannulae

Recall date: April 30, 2026Country: CACategory: medical_devices
Hazard/Reason: 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.
This page links to official sources. Verify model/lot/batch details in the official notice.