FDAJune 22, 2017device

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 h...

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

20613994900412

Recall history

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

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