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Galemed Corporation recalls Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562
Recalled January 1, 2020 · FDA recall Z-0020-2020 · Galemed
Hazard
Reports of pressure relief manifold venting gas below the standard pressure. · FDA Class I
Units
2880
Sold at
US distribution to distributors in the states of: NC and NV.
Description
Reports of pressure relief manifold venting gas below the standard pressure.
Product
Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562
Manufacturer(s)
Galemed Corporation
Made in
Taiwan
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →