Zav:ion recalls 11G BEVELED Trocar/Cannula for orthopedic/spinal procedures due to potential inadequate sterilization. Affected items may not be sterile, risking infection.
Products distributed as sterile may not have been adequately sterilized
Zav:ion is recalling 11G BEVELED Trocar/Cannula devices used in orthopedic and spinal procedures because some may not have been properly sterilized. This could lead to infection if used in medical procedures.
The devices may not have been adequately sterilized during manufacturing, which could lead to infections if used in medical procedures. This is a potential contamination risk rather than an immediate hazard.
Medical professionals using these devices in orthopedic or spinal procedures. Patients undergoing surgery with these devices are at risk of infection.
Look for the product name '11G BEVELED TROCAR/CANNULA' from Zavation. These devices are used in orthopedic and spinal procedures. The recall is pending, so no specific model numbers or dates are listed.
Verify if the device has been properly sterilized by consulting the manufacturer's guidelines or contacting Zavation directly.
The recall is due to potential inadequate sterilization of the devices, which could lead to infection if used in medical procedures.
The recall record does not specify model numbers or dates; it is pending.
Look for the product name '11G BEVELED TROCAR/CANNULA' from Zavation used in orthopedic or spinal procedures. The recall is pending, so no specific details are available.
We’ve drafted a message you can send Zav:ion to request your refund or repair — edit it as you like.
Subject: Recall Z-1736-2021 — Zav:ion Zav:ion Hello, I own a Zav:ion that is covered by recall Z-1736-2021 from Zav:ion. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.