FDANovember 27, 2018device
RESERVOIR "Y" ADAPTER, (a) BT920 (b) BT926 Suction and Anticoagulation assemblies are indicated for use with an autotransfusion system between the suction tip and reservoir.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Medtronic discovered that certain Y-connectors included in the suction lines have exhibited tearing and cracking. These defects could cause the Y-connectors to leak when in use, which could result in potential blood loss and a breach in the circuit.
What to do
FDA enforcement status: Ongoing
Brands named
medtronic perfusion systemsmedtronicmedtronic perfusion
Recall history
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