CTL Medical recalls CEZANNE II TLIF Bullet-Tip Cage (Part #018.1308) due to reports of fracturing during insertion. Affected units include specific lot numbers.
Reports received of the device fracturing during insertion.
CTL Medical is recalling their CEZANNE II TLIF Bullet-Tip Cage (Part #018.1308) because reports indicate it can fracture during insertion. This could lead to complications during spinal surgery.
The device can fracture during insertion, which may cause complications during spinal surgery. This risk occurs when the cage is being placed into the spine.
Spinal surgery patients and medical professionals using the CEZANNE II TLIF Bullet-Tip Cage for spinal fusion procedures. Those with the specific lot numbers listed are most at risk.
Check the product label for the part number 018.1308 and lot numbers 14LEDOAB, 15CNDOCC, 15DIDOBC, or 7FGBD. The device is used in spinal fusion procedures.
Look for the part number 018.1308 and lot numbers 14LEDOAB, 15CNDOCC, 15DIDOBC, or 7FGBD on the device.
The recall indicates reports of fracturing during insertion, so it is not safe to use without checking the lot numbers.
Check the product label for the part number and lot numbers; if they match, contact CTL Medical for instructions.
Look for the part number 018.1308 and lot numbers 14LEDOAB, 15CNDOCC, 15DIDOBC, or 7FGBD on the device.
We’ve drafted a message you can send CTL Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2503-2020 — CTL Medical CTL Medical Hello, I own a CTL Medical that is covered by recall Z-2503-2020 from CTL Medical. 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.