Zimmer Biomet ASI 2.0 Calcar Trimmer Shaft Recall: Potential Mating Failure

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling ASI 2.0 Calcar Trimmer Shafts for use with Zimmer Rasp Mode. The recall is because the instrument's end might not properly connect with the broach during surgery, which could lead to ineffective procedures.

Why it’s dangerous

The instrument's end may not connect properly with the broach during surgery, which could result in the trimmer not working as intended. This might cause ineffective procedures but does not pose a direct risk of injury to the patient or user.

Who’s affected

Orthopedic surgeons and surgical teams using the ASI 2.0 Calcar Trimmer Shafts with lot numbers 827310, 711160, or 203240 are affected. The risk is low as the issue is about potential inefficiency rather than immediate harm.

How to tell if you have this one

Check the lot number on the ASI 2.0 Calcar Trimmer Shaft for use with Zimmer Rasp Mode. The affected lot numbers are 827310, 711160, and 203240.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Lot Number
Identify the lot number on the ASI 2.0 Calcar Trimmer Shaft to see if it is one of the affected numbers: 827310, 711160, or 203240.

✎ GovInfoNow

Questions people ask

What is the specific problem with the ASI 2.0 Calcar Trimmer Shaft?

The end of the shaft may fail to effectively mate with the broach during surgery, which could lead to ineffective procedures.

Which lot numbers are affected?

Lot numbers 827310, 711160, and 203240 are affected.

Do I need to stop using the product?

No, the recall does not require stopping use; the issue is about potential inefficiency, not immediate safety risks.

Take action

Contact Zimmer Biomet

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

✉️ Open in email

Subject: Recall Z-0871-2020 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-0871-2020 from Zimmer 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-0871-2020 (December 19, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0871-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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.

Zimmer Biomet, Inc. recalls ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general

Lower-risk recall