FDAClass IIFebruary 25, 2026

Olympus Thunderbeat recall

Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip

Why was Olympus Thunderbeat recalled?

Firm is initiating a removal due to continued reports of adverse events.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model No. TB-0520IC; UDI: 04953170308581, 04953170608710; All Lots.

Product
Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip
Recalling firm
Olympus Corporation of the Americas
Quantity
140 units
Distribution
Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Germany, Mexico, and Japan.
Recall date
February 25, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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