Olympus recalls all Thunderbeat 5mm and 10cm Inline Grip devices due to safety concerns from adverse events. Learn what to do.
Firm is initiating a removal due to continued reports of adverse events.
Olympus is recalling all Thunderbeat 5mm and 10cm Inline Grip devices because of reports of adverse events. This recall means the product may pose safety risks that require immediate attention.
The recall is initiated due to continued reports of adverse events. However, the specific hazard mechanism is not clearly described in the notice.
Users of the Olympus Thunderbeat 5mm and 10cm Inline Grip devices are affected. Those who have purchased these products are most at risk.
Check for the model number TB-0510IC and unique device identifier UDI: 04953170308734 on the product. All units of this device are affected.
Look for the model number TB-0510IC and unique device identifier UDI: 04953170308734 on the product.
The recall is initiated due to continued reports of adverse events.
Check for the model number TB-0510IC and unique device identifier UDI: 04953170308734 on the product.
The recall notice does not specify a remedy.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1382-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1382-2026 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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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.
