Olympus recalls Thunderbeat 5mm 20cm Front-Actuated Grip due to reported safety issues. Affected units include all lots with specific model and lot codes.
Firm is initiating a removal due to continued reports of adverse events.
Olymp: Olympus is recalling its Thunderbeat 5mm, 20cm Front-Actuated Grip devices due to continued reports of adverse events. This recall is important because the product has been linked to safety concerns that require immediate attention.
The hazard is described as 'continued reports of adverse events,' but the specific mechanism causing harm is not detailed in the recall notice. The hazard is not clearly defined to indicate a specific risk like injury or damage.
Users of the Olympus Thunderbeat 5mm, 20cm Front-Actuated Grip devices are affected. Individuals who purchased the product from any retailer are most at risk.
Check for the model code TB-0520FC and lot codes 04953170370519 or 04953170370502 on the product. All lots of this device are included in the recall.
Identify the model code TB-0520FC and lot codes 04953170370519 or 04953170370502 to confirm if your device is affected.
The recall notice does not mention any remedy or fix for the product.
Check for the model code TB-0520FC and lot codes 04953170370519 or 04953170370502 on the product.
The recall notice does not specify any action steps for affected devices.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1376-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1376-2026 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.
