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Recall Observatory FDA recall evidence

Device product

DLP Cardioplegia Adapter with Pressure Port Provides access for a pressure monitoring needle near the connection to the cardioplegia cannula. These adapters are intended for use in conjunction with the delivery of cardioplegia solution and to provide access for pressure monitoring for up to six hours

Z-2766-2017

June 22, 2017

Class II

Product summary

Firm
Medtronic Perfusion Systems
Event
Event 77641
Status
Terminated
Classification
Class II
Quantity
63053 (48180 US) (14873 OUS)
Official record key
device-enforcement:Z-2766-2017

Official wording

Reason: Identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.

Code information: Model No. 15004; Product UPN 20613994900412; Lot No. 2016031072, 2016031509, 2016050243, 2016081219, 2016100630, 2016120083, 2016120448, 2017040113.

Distribution pattern: Worldwide Distribution - US (nationwide) Foreign: Argentina, Australia, Austria, Belgium, Bulgaria, Canada, Croatia, Denmark, El Salvador, France, Georgia, Germany, Hungary, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Macedonia, Moldova, Netherlands, New Zealand, Nigeria, Norway, Poland, Romania, Russian Federation, Slovenia, Spain, Thailand, Turkey, & United Kingdom.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.