FDAAugust 18, 2015device

MEDTRONIC PERFUSION TUBING PACKS (with potentially affected Hemoconcentrators). Model # 7U65R2, 8C72R4, 6N21R2, BB7M38R11, TL2Q68R17, HY8R66R3, HY2U43R9, 8C72R4, BB5J59R19, 6B65R3, TL7M46R7, TL2Q68R17, 7U65R2, M074704B, M230002A, BB7M38Rll, M450013B, BB8N86R4, HY2U43R9, 8C72R4, M650123A, HY8R55R ...

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

The hazard

Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration performance that is below product specification. These potentially affected units have been distributed as stand-alone devices and in specific lots of Medtronic Perfusion Tubing packs.

What to do

FDA enforcement status: Terminated

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

Recall history

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

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