Biomet Healing Abutment Recall: Incorrect Rotation Risk

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Recalling firmBiomet 3i, LLC4555 Riverside Dr, N/A · Palm Beach Gardens, FL 33410-4200

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Biomet is recalling certain Healing Abutments that may cause dental implants to rotate incorrectly by up to 30 degrees. This could lead to misaligned margins and improper healing.

Why it’s dangerous

The Healing Abutment may produce scanned data that rotates dental implants by about 30 degrees. This misalignment could cause improper healing and margin issues.

Who’s affected

Dental patients with the specific lot numbers (1228593, 1230791) who received the Healing Abutment. Patients with dental implants are most at risk.

How to tell if you have this one

Check for the model 'Healing Abutment 5MM(D) X 6MM(P) X 3MM(H)' with lot numbers 1228593 or 1230791. The reference number is IEHA563.

Brand
Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the lot numbers (1228593 or 1230791) and reference number IEHA563 on your Healing Abutment.

✎ GovInfoNow

Questions people ask

What is the specific model of Healing Abutment being recalled?

The specific model is the Healing Abutment 5MM(D) X 6MM(P) X 3MM(H) with reference number IEHA563.

What lot numbers are affected?

Lot numbers 1228593 and 1230791 are affected.

Is there a fix for this issue?

The recall record does not mention any remedy or fix.

Take action

Contact Biomet

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

✉️ Open in email

Subject: Recall Z-1384-2020 — Biomet Biomet

Hello,

I own a Biomet that is covered by recall Z-1384-2020 from Biomet.

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-1384-2020 (January 10, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1384-2020 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.

Biomet 3i, LLC recalls CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 3MM(H) Reference Number: IEHA563

Lower-risk recall