Medicrea TLIF-B Holder Recall: Risk of Separated Draw Rod

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Recalling firmMedicrea International5389 Route De Strasbourg, Vancia · Rillieux La Pape, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Medicrea is recalling its TLIF-B Holders (Catalog A24200010) because the inner draw rod might separate from the proximal knob during use. This could lead to improper spinal fusion procedures if not addressed.

Why it’s dangerous

The inner draw rod may separate from the proximal knob during use, potentially causing the holder to become unstable. This could affect the precision of spinal fusion surgery if the rod does not stay securely attached.

Who’s affected

Surgical patients and healthcare providers who use the Medicrea TLIF-B Holder for spinal fusion procedures. Those with Lot Numbers l9B0570 or l9B0572 are most at risk.

How to tell if you have this one

Check for the Medicrea TLIF-B Holder with Catalog Number A24200010 and Lot Numbers l9B0570 or l9B0572. This product is used in spinal fusion procedures.

Brand
Medicrea
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the Catalog Number A24200010 and Lot Numbers l9B0570 or l9B0572 on the device.

✎ GovInfoNow

Questions people ask

What is the recall for?

Medicrea recalls its TLIF-B Holders (Catalog A24200010) with Lot Numbers l9B0570 or l9B0572 due to potential separation of the inner draw rod from the proximal knob.

Is there a fix for this issue?

The recall record does not mention any remedy or fix for this issue.

Who should contact for help?

The recall record does not specify a contact for assistance.

Take action

Contact Medicrea

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

✉️ Open in email

Subject: Recall Z-1156-2020 — Medicrea Medicrea

Hello,

I own a Medicrea that is covered by recall Z-1156-2020 from Medicrea.

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-1156-2020 (October 2, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1156-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Medicrea International recalls Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010

Lower-risk recall