Olympus Thunderbeat Hand Instruments May Have Damaged Probe Tips

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Recalling firmOlympus Corporation of the Americas3500 Corporate Pkwy · Center Valley, PA 18034-8229

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling Thunderbeat hand instruments that may have damaged or detached probe tips. This could cause injury during medical procedures if the instrument fails unexpectedly.

Why it’s dangerous

The probe tips can become damaged or detach during use, potentially causing injury if the instrument malfunctions. This is a risk during medical procedures where the instrument is used for precise tissue manipulation.

Who’s affected

Medical professionals using Olympus Thunderbeat instruments with ultrasonic or electrosurgical generators. Patients undergoing procedures with these instruments may be at risk if the probe fails.

How to tell if you have this one

Check for model number TB-0520FCS on the instrument. These instruments were sold with USG-400 or WSG-400 generators and have catalog number N5423930.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Instrument Model
Look for model number TB-0520FCS on the instrument to confirm it is affected.
Contact Manufacturer
Reach out to Olympus Corporation of the Americas for guidance on next steps.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The probe tips of the hand instruments may be damaged or breaking, including pad damage and detachment.

What should I do if I have this product?

Check the model number on the instrument. If it is TB-0520FCS, contact Olympus Corporation of the Americas for guidance.

Are there any safety risks?

Yes, damaged or detached probe tips could cause injury during medical procedures.

Take action

Contact Olympus

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

✉️ Open in email

Subject: Recall Z-1001-2025 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1001-2025 from Olympus.

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-1001-2025 (November 25, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1001-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Olympus Corporation of the Americas recalls Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm,

Lower-risk recall