Zimmer Biomet ARCOS Hip Stem Recall: Risk of Longer Surgery Time

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Contact the company & request your remedy

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

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling a hip stem product due to possible mixing of components, which could lead to longer surgery times to find the correct replacement part.

Why it’s dangerous

The recall involves two lots of hip stems that may have been mixed together. This could cause surgeons to spend extra time locating the correct replacement component during surgery.

Who’s affected

Patients who received the ARCOS Modular Revision Hip System with item number 11-300814 and lot 621550 are affected. Those with hip replacements using this specific stem are at risk.

How to tell if you have this one

Check for the product name 'ARCOS Modular Revision Hip System' and item number 11-300814. The specific lot number 621550 is also associated with this recall.

Brand
Zimmer Biomet
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Review the item number and lot number on your hip stem to confirm if it matches the recalled product.

✎ GovInfoNow

Questions people ask

Why is this hip stem being recalled?

The recall is due to potential mixing of two lots of the hip stem, which could lead to extended surgery time to find the correct replacement component.

What should I do if I have this hip stem?

The official recall notice does not specify a remedy or action for affected individuals.

Is there a risk of serious injury from this recall?

The recall describes potential for longer surgery time but does not mention serious injury 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-2820-2018 — Zimmer Biomet Zimmer Biomet

Hello,

I own a Zimmer Biomet that is covered by recall Z-2820-2018 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-2820-2018 (June 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2820-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 21, 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 ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.

Lower-risk recall