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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling Thunderbeat 5mm hand instruments that may have damaged or broken probe tips. This could lead to pad detachment or improper function during surgery. Affected items have model TB-0545FCS and catalog number N5423330.

Why it’s dangerous

The probe tips of these hand instruments can become damaged or break, causing pad detachment. This may lead to improper function during surgical procedures but does not typically cause injury.

Who’s affected

Surgical staff and hospitals using Olympus Thunderbeat 5mm hand instruments with model TB-0545FCS are affected. The risk is low as the hazard involves potential probe tip damage but not immediate injury.

How to tell if you have this one

Check for model number TB-0545FCS or catalog number N5423330 on the instrument. The product was sold with all lots and is part of the Thunderbeat 5mm, 45 cm, Front-actuated Grip Type S series.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Damaged Probe Tips
Inspect the instrument for broken or detached probe tips, which may indicate damage.

✎ GovInfoNow

Questions people ask

Do I need to stop using these instruments?

The recall does not require immediate stop use; however, check for damaged probe tips before use.

What should I do if I find damaged probe tips?

The recall does not specify a remedy, so contact Olympus directly for guidance.

Are there any specific model numbers affected?

Yes, model TB-0545FCS and catalog number N5423330 are affected.

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-0998-2025 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-0998-2025 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-0998-2025 (November 25, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0998-2025 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,45

Lower-risk recall