FDAApril 27, 2021device

The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits. Model: BB14

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

The hazard

The device is used as part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits and may collapse during use which can increase resistance to flow in the venous line and cause a drop in circuit blood flow.

What to do

FDA enforcement status: Ongoing

Brands named

circulatory technologycirculatory

UPCs

00851997007004

Recall history

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

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