CTL Medical CEZANNE II TLIF Cage Fractures During Insertion

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Recalling firmCTL Medical Corporation4550 Excel Pkwy Ste 300 · Addison, TX 75001-5714

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✎ GovInfoNow plain-language explainer

What happened, in plain English

CTL Medical is recalling a spinal surgery device called the CEZANNE II TLIF Bullet-Tip Cage because reports indicate it can fracture while being inserted. This could lead to complications during surgery if the device breaks unexpectedly.

Why it’s dangerous

The device can fracture during insertion, which may cause complications during spinal surgery. This risk occurs when the device is being placed into the spine by a medical professional.

Who’s affected

Surgical teams and patients undergoing spinal fusion procedures using the recalled device. Those with the specific lot numbers are most at risk.

How to tell if you have this one

Check the product label for part number 018.1307 and lot numbers 14LDDOCB, 15CNDOBC, 15DIDOCC, or 7FGAD. The device is used in spinal fusion surgeries.

Brand
CTL Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Label
Look for part number 018.1307 and lot numbers 14LDDOCB, 15CNDOBC, 15DIDOCC, or 7FGAD on the device.

✎ GovInfoNow

Questions people ask

Why is this device being recalled?

Reports received of the device fracturing during insertion.

What should I do if I have this device?

Check the device label for part number 018.1307 and lot numbers 14LDDOCB, 15CNDOBC, 15DIDOCC, or 7FGAD. If you have these, contact CTL Medical for guidance.

Is there a fix for this problem?

The recall record does not mention a remedy or fix.

Take action

Contact CTL Medical

We’ve drafted a message you can send CTL Medical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2501-2020 — CTL Medical CTL Medical

Hello,

I own a CTL Medical that is covered by recall Z-2501-2020 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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Where this comes from

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.

Official source: FDA Recall #Z-2501-2020 (August 21, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2501-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

CTL Medical Corporation recalls CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H7mm, Part #018.1307.

Use caution until it’s fixed