Olympus recalls Thunderbeat 5mm 20cm front-actuated grip models due to reported safety issues. Affected units include specific model numbers and lots. Consumers should check their product details.
Firm is initiating a removal due to continued reports of adverse events.
Olympus is recalling its Thunderbeat 5mm, 20cm, Front-Actuated Grip Type S devices because of continued reports of adverse events. This recall affects specific model numbers and lots sold globally. The hazard involves potential safety risks that require immediate attention.
The recall is initiated due to continued reports of adverse events. While the exact nature of the adverse events isn't specified, the company is taking action to remove these products from circulation to prevent potential safety issues.
Owners of Olympus Thunderbeat 5mm, 20cm, Front-Actuated Grip Type S devices with model numbers TB-0520FCS and specific lot numbers are affected. Users who have these devices should check if they are included in the recall.
Check for the model number TB-0520FCS on your Olympus Thunderbeat device. Look for the unique device identifiers (UDIs) listed: 04953170383571, 0495317083595, 04953170383588. All lots of this product are affected.
Identify your Olympus Thunderbeat device's model number and unique device identifiers (UDIs) to confirm if it is affected.
Olympus is initiating a removal due to continued reports of adverse events.
Model number TB-0520FCS with unique device identifiers (UDIs) 04953170383571, 0495317083595, 04953170383588.
The recall does not specify a stop-use instruction; check your product details to see if it is affected.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1373-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1373-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
