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Zavation recalls InterV 11G Kyphoplasty Kit, REF Numbers: a) INTVMN-10-DSK b) INTVMN-15-DSK c) INTVMN-15-DSKC d) INTVMN-20-DSK. F
Recalled June 9, 2021 · FDA recall Z-1755-2021 · Zavation
Hazard
Products distributed as sterile may not have been adequately sterilized · FDA Class II
Units
119 units
Sold at
US nationwide distribution.
Description
Products distributed as sterile may not have been adequately sterilized
Product
InterV 11G Kyphoplasty Kit, REF Numbers: a) INTVMN-10-DSK b) INTVMN-15-DSK c) INTVMN-15-DSKC d) INTVMN-20-DSK. For use in Orthopedic / spinal procedures.
Manufacturer(s)
Zavation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →