Sybron Legacy 3 Dental Implant Recall: Incorrect Implants May Cause Surgery Rescheduling

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Contact the company & request your remedy

Recalling firmImplant Direct Sybron Manufacturing LLC3050 E Hillcrest Dr, N/A · Westlake Village, CA 91362-3171

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Sybron is recalling Legacy 3 dental implants that may have incorrect sizes, which could lead to surgery rescheduling. This affects patients who received the specific model with the described dimensions and lot number.

Why it’s dangerous

The implants may have incorrect dimensions, causing the need for surgery rescheduling. This happens because the wrong size could affect the implant's fit and function during dental procedures.

Who’s affected

Patients who received the Legacy 3 implant with size 4.2mmD x 13mmL and platform 3.5mmD (lot 83327) are affected. Dental professionals who used this specific model during procedures are at risk.

How to tell if you have this one

Check for the Legacy 3 implant with size 4.2mmD x 13mmL, platform 3.5mmD, and lot number 83327. The product is sold under Sybron Manufacturing LLC.

Brand
Sybron
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Implant Details
Verify the implant size, platform, and lot number to confirm if it matches the recalled model.

✎ GovInfoNow

Questions people ask

Why is this implant being recalled?

The recall is due to incorrect implant sizes that could lead to surgery rescheduling.

What should I do if I have this implant?

Check the implant details to see if it matches the recalled model; no immediate action is required beyond verification.

Is there a fix for this issue?

The official recall does not mention a fix or remedy; affected patients may need to reschedule surgery.

Take action

Contact Sybron

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

✉️ Open in email

Subject: Recall Z-1041-2020 — Sybron Sybron

Hello,

I own a Sybron that is covered by recall Z-1041-2020 from Sybron.

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-1041-2020 (October 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1041-2020 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.

Implant Direct Sybron Manufacturing LLC recalls Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213

Lower-risk recall