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Recall Observatory FDA recall evidence

Device product

InterV CurvePlus Kit, REF Numbers: a) INTVMC-15-FLDSK b) INTVMC-20-FLDSK. For use in Orthopedic / spinal procedures.

Z-1753-2021

March 25, 2021

Class II

Product summary

Firm
Zavation
Event
Event 87661
Status
Terminated
Classification
Class II
Quantity
36 units
Official record key
device-enforcement:Z-1753-2021

Official wording

Reason: Products distributed as sterile may not have been adequately sterilized

Code information: a) INTVMC-15-FLDSK, Lot Numbers: 10659ZV b) INTVMC-20-FLDSK, Lot Numbers: 10312ZV, 11698ZV, 10276ZV, 10205ZV, 10031ZV

Distribution pattern: US nationwide distribution.

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    may not have been adequately sterilized