Olympus recalls Thunderbeat 5mm 35cm Front-Actuated Grip due to safety concerns. Affected units include all lots with model TB-0535FC and UDI numbers starting 04953170337574 or 049:53170464959.
Firm is initiating a removal due to continued reports of adverse events.
Olympus is recalling its Thunderbeat 5mm, 35cm, Front-Actuated Grip due to reports of adverse events. This recall affects all units with the specified model and unique identifiers. Consumers should check their product details to determine if they are affected.
The recall is initiated due to continued reports of adverse events. However, the specific nature of these events and the exact hazard mechanism are not clearly described in the official notice.
Owners of the Olympus Thunderbeat 5mm, 35cm, Front-Actuated Grip with model number TB-0535FC and the listed unique identifiers are affected. Users of this product are most at risk if they have the recalled units.
Check for the model number TB-0535FC and unique identifiers starting with 04953170337574 or 04953170464959 on the product. All lots of this specific model are included in the recall.
Identify if your Olympus Thunderbeat 5mm, 35cm, Front-Actuated Grip has the model number TB-0535FC and the listed unique identifiers.
The recall is initiated due to continued reports of adverse events, but the specific hazard mechanism is not clearly described in the official notice.
Check for the model number TB-0535FC and unique identifiers starting with 04953170337574 or 04953170464959 on the product. All lots of this model are affected.
The official notice does not specify a remedy for this recall, so no action is required beyond checking if your product 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-1375-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1375-2026 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.
