Olympus recalls Thunderbeat 5mm 35cm Inline Grip due to reported safety issues. Affected units include all lots with model TB-0535IC.
Firm is initiating a removal due to continued reports of adverse events.
Olympus is recalling its Thunderbeat 5mm 35cm Inline Grip product due to continued reports of adverse events. This recall affects all units with model number TB-053:0535IC.
The hazard is described as continued reports of adverse events, but the specific mechanism is not detailed in the recall notice. The exact nature of the adverse events is unclear.
Users of the Olympus Thunderbeat 5mm 35cm Inline Grip are affected. Those who have purchased this product are most at risk.
Check for the model number TB-0535IC on the product. The product was sold with a unique device identifier (UDI) starting with 04953170464973.
Look for the model number TB-0535IC and unique device identifier starting with 04953170464973.
The recall states there are continued reports of adverse events, but the specific hazard is not detailed.
The recall does not specify a remedy, so no action is required beyond checking if you have the product.
Check for the model number TB-0535IC and unique device identifier starting with 04953170464973.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1380-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1380-2026 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.
