FDAJune 22, 2017device

DLP Extension Line Adapters 20 in length Used to extend cardioplegia line during cardiopulmonary bypass surgery

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

20613994918554

Recall history

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

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