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Use caution Medical device recall · FDA · Published September 4, 2018

Leica M525 F20 Surgical Microscope System Recall: Risk of Tipping Over

Leica recalls M525 F20 Surgical Microscope System with serial numbers listed. The instrument may tip over when swing arm is fully extended, causing potential injury.

🇺🇸 FDA recall #Z-3175-2018Medical deviceLeica ›
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Recalling firmLeica Microsystems, Inc.1700 Leider Ln · Buffalo Grove, IL 60089-6622
✎ GovInfoNow plain-language explainer

What happened, in plain English

Leica is recalling its M525 F20 Surgical Microscope System due to complaints that it tips over when the swing arm is fully extended. This could lead to injury if the microscope falls during use. Read more at govinfonow.com/recall/69918-leica-m525-f20-surgical-microscope-system-recall-risk-of-tipping.

Source Summary by GovInfoNow · govinfonow.com/recall/69918-leica-m525-f20-surgical-microscope-system-recall-risk-of-tipping · Updated August 20, 2026 · FDA enforcement record: FDA #Z-3175-2018

Cite this page

“Leica M525 F20 Surgical Microscope System Recall: Risk of Tipping Over.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69918-leica-m525-f20-surgical-microscope-system-recall-risk-of-tipping. Based on FDA recall #Z-3175-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3175-2018%22&limit=1).

Why it’s dangerous

The microscope's swing arm can tip over when fully extended, potentially causing injury if it falls on a person or equipment. This hazard is reported through user complaints but does not indicate a specific mechanism for causing serious injury.

Who’s affected

Surgical professionals and medical facilities that own or use the Leica M525 F20 Surgical Microscope System with the listed serial numbers are most at risk. The hazard occurs during routine use when the swing arm is fully extended.

How to tell if you have this one

Check the serial number on your Leica M525 F20 Surgical Microscope System. The affected units have specific serial numbers listed in the recall notice, including those added in October 2018.

  • Brand
    Leica
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Serial Number

    Identify your microscope's serial number to see if it matches the list provided in the recall notice.

How this recall unfolded

Recall timeline

FDA terminated this recall 3 years after the firm started it.

1. Firm started the recall: Sep 4, 201812. FDA classified it Class II: Sep 14, 201823. Published in FDA’s Enforcement Report: Sep 26, 201834. FDA terminated the recall: Aug 17, 2021420182021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Questions people ask

What should I do if I have this microscope?

Check your serial number against the list provided in the recall notice. If it matches, stop using it until you can contact Leica for further instructions.

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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-3175-2018 (September 4, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3175-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 20, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA