Olympus recalls Thunderbeat 5mm 45cm Front-Actuated Grip due to reported safety issues. Affected units include all lots with model TB-0545FC.
Firm is initiating a removal due to continued reports of adverse events.
Olymp: Olympus is recalling its Thunderbeat 5mm 45cm Front-Actuated Grip because of continued reports of adverse events. This recall affects all units with model number TB-0545FC.
The hazard is described as 'continued reports of adverse events,' but the specific nature of these events is not detailed in the recall notice. Without clear information on the cause or mechanism, the exact danger level cannot be determined.
Users of the Olympus Thunderbeat 5mm 45cm Front-Actuated Grip are affected. Those who have purchased this product are most at risk.
Check for the model number TB-0545FC on the product. The product was sold with a unique device identifier (UDI) 04953170337543 and all lots are affected.
Identify the model number TB-0545FC and UDI 04953170337543 to confirm if your product is affected.
The recall is initiated due to continued reports of adverse events, but the specific nature of these events is not detailed in the notice.
The recall notice does not specify a remedy, so check the product details to confirm if it is affected.
The recall notice does not provide a deadline for action.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1374-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1374-2026 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.
