CanadaMedtronic DLP Retrograde Cardioplegia Cannulae (Medtronic Inc.), model/catalogue number 94113T, with lot/serial numbers 0231757975, 0231667046, and 0231651336 are affected. On 8 January 2026 Medtronic received a complaint that the chevron-side seal of pouches was not fully sealed and opened to air, and 17 cannulae were identified as unsterile; contact the manufacturer for additional information.
What's being recalled
Companies: Medtronic Inc., 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432.
How to identify it
Affected products: DLP Retrograde Cardioplegia Cannulae; Lot or serial number: 0231757975; Model or catalogue number: 94113T
Affected products: DLP Retrograde Cardioplegia Cannulae; Lot or serial number: 0231667046; Model or catalogue number: 94113T
Affected products: DLP Retrograde Cardioplegia Cannulae; Lot or serial number: 0231651336; Model or catalogue number: 94113T
The hazard
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.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)