FDASeptember 22, 2017device

Better-Bladder cardiopulmonary bypass blood reservoir; Models: BB14 (individual, sterile, pouched) and BB14NS (sold bulk to kit manufacturers)

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: Terminated

Brands named

circulatory technologycirculatory

Recall history

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

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