Zavation recalls InterV CurvePlus Kit (REF numbers INTVMC-15-FLDSK and INTVMC-20-FLDSK) due to potential inadequate sterilization of sterile products used in orthopedic/spinal procedures. Affected units include specific lot numbers.
Products distributed as sterile may not have been adequately sterilized
Zavation is recalling InterV CurvePlus Kits used in orthopedic or spinal procedures because some products may not have been properly sterilized. This could lead to infections or other complications if used in medical procedures.
The kits are designed for sterile medical procedures, but some units may not have been adequately sterilized. This could lead to infections or other complications if used during surgery.
Healthcare professionals using the InterV CurvePlus Kit for orthopedic or spinal procedures are most at risk. Patients receiving these kits during surgery may also be affected if the kit was not properly sterilized.
Check for REF numbers: INTVMC-15-FLDSK or INTVMC-20-FLDSK. Lot numbers for these kits include 10659ZV (for INTVMC-15-FLDSK) and 10312ZV, 11698ZV, 10276ZV, 10205ZV, 10031ZV (for INTVMC-20-FLDSK).
Look for lot numbers: 10659ZV for INTVMC-15-FLDSK and 10312ZV, 11698ZV, 10276ZV, 10205ZV, 10031ZV for INTVMC-20-FLDSK.
The kits may not have been adequately sterilized, which could lead to infections or complications during medical procedures.
Check the lot numbers to see if your kit is affected. If it is, contact Zavation for instructions.
Yes, if the kit was not properly sterilized, it could cause infections or other complications during surgery.
We’ve drafted a message you can send Zavation to request your refund or repair — edit it as you like.
Subject: Recall Z-1753-2021 — Zavation Zavation Hello, I own a Zavation that is covered by recall Z-1753-2021 from Zavation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
