FDAMarch 25, 2021device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Products distributed as sterile may not have been adequately sterilized

What to do

FDA enforcement status: Terminated

Brands named

zavation

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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. — Recall Details · AllClear