Globus Medical ALTERA Spacer Recall: Stainless Steel Risk

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Recalling firmGlobus Medical, Inc.2560 General Armistead Ave, N/A · Audubon, PA 19403-5214

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Globus Medical is recalling specific lots of ALTERA Spacer implants because they may contain stainless steel instead of the intended cobalt chromium molybdenum alloy. This could lead to complications if the implant fails during surgery.

Why it’s dangerous

The implants may have been made with stainless steel instead of the specified cobalt chromium molybdenum alloy. This difference in material could cause the implant to fail during surgery, potentially leading to complications for the patient.

Who’s affected

Patients who received the recalled ALTERA Spacer implants during surgery are likely affected. Surgeons and medical facilities using these specific lots should be cautious.

How to tell if you have this one

Check the implant's lot number on the packaging or documentation. The recalled lots include specific identifiers: GBX132UC / (01)00889095720723(17)250511(10)GBX132UC.

Brand
Globus Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Implant Details
Review the implant's lot number and part number to determine if it matches the recalled identifiers.

✎ GovInfoNow

Questions people ask

What is the specific hazard with these implants?

The implants may contain stainless steel instead of the specified cobalt chromium molybdenum alloy, which could lead to failure during surgery.

How can I tell if my implant is recalled?

Check the lot number on the implant packaging or documentation; recalled lots include GBX132UC / (01)00889095720723(17)250511(10)GBX132UC.

What should I do if I have the recalled implant?

The recall record does not specify a remedy, so contact Globus Medical directly for guidance.

Take action

Contact Globus Medical

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

✉️ Open in email

Subject: Recall Z-2850-2020 — Globus Medical Globus Medical

Hello,

I own a Globus Medical that is covered by recall Z-2850-2020 from Globus Medical.

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-2850-2020 (July 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2850-2020 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.

Globus Medical, Inc. recalls ALTERA Spacer ALTERA Spacer, 10x31, 8-12mm, 8¿ (sterile)

Recall notice