Biomet Regener: Primary Taper Cap Not Sterilized Risk

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Contact the company & request your remedy

Recalling firmBiomet, Inc.56 E Bell Dr, N/A · Warsaw, IN 46582-6989

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Biomet is recalling its Regenerex Primary Taper Cap (Item 141269) because it may not have been properly sterilized. This could lead to infection risks if used in medical procedures. Affected units have specific lot numbers listed in the recall.

Why it’s dangerous

The product may not be properly sterilized due to alignment issues with the gamma sterilization process. This could lead to infection if used in medical procedures without proper sterilization.

Who’s affected

Medical professionals using the Regenerex Primary Taper Cap for surgical procedures. Patients undergoing surgery with this cap may be at risk if the product wasn't properly sterilized.

How to tell if you have this one

Check the product label for Item Number 141269 and Lot Numbers: 015800, 324440, 685300, 023900, 324440R, 696280, 058930, 389060, 821980, 200720, 418430, 890320, 313260, 646040, 997610.

Brand
Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for Item Number 141269 and the listed lot numbers on the product.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The product may not be properly sterilized due to alignment issues with the gamma sterilization process.

What should I do if I have this product?

Check the product label for Item Number 141269 and the listed lot numbers. Contact Biomet for further instructions.

Is there a risk of serious injury?

The recall is for potential infection risk if the product wasn't properly sterilized, but no specific injury mechanism is described.

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-0081-2021 — Biomet Biomet

Hello,

I own a Biomet that is covered by recall Z-0081-2021 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-0081-2021 (September 4, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0081-2021 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, Inc. recalls Biomet Regenerex Primary Taper Cap Item Number 141269

Lower-risk recall