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Zavation recalls InterV CurvePlus Kit, REF Numbers: a) INTVMC-15-FLDSK b) INTVMC-20-FLDSK. For use in Orthopedic / spinal procedures.
Recalled June 9, 2021 · FDA recall Z-1753-2021 · Zavation
Hazard
Products distributed as sterile may not have been adequately sterilized · FDA Class II
Units
36 units
Sold at
US nationwide distribution.
Description
Products distributed as sterile may not have been adequately sterilized
Product
InterV CurvePlus Kit, REF Numbers: a) INTVMC-15-FLDSK b) INTVMC-20-FLDSK. For use in Orthopedic / spinal procedures.
Manufacturer(s)
Zavation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →