FDAMay 30, 2019device
Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Reports of pressure relief manifold venting gas below the standard pressure.
What to do
FDA enforcement status: Terminated
Brands named
galemed
UPCs
04710810093562
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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