FDAJune 22, 2017device

DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with flexible lines and standard luer sites to facilitate direct connections to the cannulae

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

20613994677611

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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