FDAApril 29, 2021device

Medtronic CB10Y89R10, Custom Pack CB10Y89R10 ECC 3/8 A/V, Custom Perfusion System, Sterile, Rx.

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

The hazard

Specific lots may have been manufactured with insufficient or incomplete welds.

What to do

FDA enforcement status: Terminated

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

00763000499105

Recall history

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

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