GaleMed Corporation Issues Nationwide Recall of Babi.Plus ...
On May 27, 2019, GaleMed Corporation initiated a nationwide recall of the Babi.Plus 12.5cmH 2 O Pressure Relief Manifold. A total of 29,844 units are subject to the recall. GaleMed Corporation has notified the FDA of this action. Device Use: The Babi.Plus Pressure Relief Manifold is a single patient use device intended for use with humans ................
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