FDAJuly 9, 2024device

Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312

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

The hazard

During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).

What to do

FDA enforcement status: Ongoing

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

20613994879329

Recall history

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

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