Olympus Thunderbeat 5mm 20cm Inline Grip Recall: Safety Concerns

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Contact the company & request your remedy

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 its Thunderbeat 5mm 20cm Inline Grip device because of continued reports of adverse events. This recall affects all units sold and requires customers to stop using the product until further notice.

Why it’s dangerous

The recall is initiated due to continued reports of adverse events. The exact nature of these events is not specified in the notice, so the specific hazard mechanism remains unclear.

Who’s affected

All owners of the Olympus Thunderbeat 5mm 20cm Inline Grip device are affected. Users with this specific model are most at risk due to the reported adverse events.

How to tell if you have this one

Check for the model number TB-0520IC and unique device identifier (UDI) numbers 04953170308581 or 04953170608710. All lots of this product are included in the recall.

Brand
Olympus
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop Using It Now
Immediately stop using the Olympus Thunderbeat 5mm 20cm Inline Grip device as it is being recalled due to adverse events.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The recall is initiated due to continued reports of adverse events, but the specific nature of these events is not detailed in the notice.

What models are affected?

All Olympus Thunderbeat 5mm 20cm Inline Grip devices with model number TB-0520IC and UDI numbers 04953170308581 or 04953170608710 are affected.

How can I check if my product is recalled?

Check for the model number TB-0520IC and unique device identifier (UDI) numbers 04953170308581 or 04953170608710 on your device.

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-1381-2026 — Olympus Olympus

Hello,

I own a Olympus that is covered by recall Z-1381-2026 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-1381-2026 (October 22, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1381-2026 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 Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip

Recall notice