Olympus Thunderbeat II Shears Recall: Distal Tip Detachment Risk

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Contact the company & request your remedy

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Olympus is recalling Thunderbeat II Shears with Ultrasonic Mode (model TB2-0520FC) because a part could detach during use. This could lead to injury if the detached part causes a cut or other harm. Owners should stop using the shears immediately and contact Olympus for a fix.

Why it’s dangerous

The shears' distal tip component can become detached during normal use. If the tip separates, it may cause a cut or injury to the user or others nearby. This risk is higher when the shears are used for precise cutting tasks.

Who’s affected

Users of Olympus Thunderbeat II Shears with Ultrasonic Mode (model TB2-0520FC) are affected. People who use these shears for hair cutting or similar tasks are most at risk.

How to tell if you have this one

Check for the model number TB2-0520FC on the shears. The product was sold with UDI-DI number 04953170439995 and all lot numbers.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using Shears Now
Immediately stop using the Olympus Thunderbeat II Shears with Ultrasonic Mode (model TB2-0520FC) to prevent potential injury from a detached tip.

✎ GovInfoNow

Questions people ask

What is the model number of the recalled shears?

The model number is TB2-0520FC.

How can I tell if my shears are affected?

Check for the model number TB2-0520FC on the shears. The product was sold with UDI-DI number 04953170439995 and all lot numbers.

What should I do if I have the recalled shears?

Stop using the shears immediately and contact Olympus for a fix or replacement.

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-1851-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1851-2026 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-1851-2026 (March 23, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1851-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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 Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.

Use caution until it’s fixed