Public recall detail

Medtronic DLP Retrograde Cardioplegia Cannulae

2026-04-30

medium
Cardiovascular Sterility
Quick summary

Quick summary: Medtronic DLP Retrograde Cardioplegia Cannulae. Reason: Sterility. Category: Cardiovascular. Date: 2026-04-30.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Medtronic DLP Retrograde Cardioplegia Cannulae. Reason: Sterility. Category: Cardiovascular. Date: 2026-04-30.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandMEDTRONIC INC.
ProductMedtronic DLP Retrograde Cardioplegia Cannulae
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-82009

Affected products

ProductDLP Retrograde Cardioplegia Cannulae
Lot0231757975
Model94113T
Serial number0231757975
DescriptionDLP Retrograde Cardioplegia Cannulae
ProductDLP Retrograde Cardioplegia Cannulae
Lot0231667046
Model94113T
Serial number0231667046
DescriptionDLP Retrograde Cardioplegia Cannulae
ProductDLP Retrograde Cardioplegia Cannulae
Lot0231651336
Model94113T
Serial number0231651336
DescriptionDLP Retrograde Cardioplegia Cannulae

Issue

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 you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesMedtronic Inc. 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
Recall date2026-04-21
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82009
Background{}
CompaniesMedtronic Inc. 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
AudiencesHealthcare
Source updated2026-04-30

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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