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InfuTronix LLC recalls Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a conta
Recalled July 31, 2019 · FDA recall Z-2055-2019 · InfuTronix
Hazard
Potential for tube leakage · FDA Class II
Units
10,800 units
Sold at
US distribution in the state of MA
Description
Potential for tube leakage
Product
Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a needle or a catheter.
Manufacturer(s)
InfuTronix LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →