Olympus recalls OER-Pro devices due to safety warnings and maintenance cautions. Affected units require proper training for repairs and adherence to maintenance schedules.
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
Olymp: Olympus is recalling its OER-Pro devices because they require specific safety warnings and maintenance procedures. This recall emphasizes that only trained personnel should handle repairs to prevent risks.
The hazard involves potential risks if devices are not maintained correctly or repaired by trained personnel. Improper handling could lead to safety issues, though the specific mechanism isn't detailed in the recall.
Users of Olympus OER-Pro devices are affected. Those who have not followed proper maintenance schedules or attempted repairs without training are at higher risk.
Check for the model 'OER-Pro' on the device. The recall covers all units with the serial number range specified in the UDI: 04953170258589.
Read the device's safety warnings and cautions provided by Olympus.
Adhere to the manufacturer's recommended maintenance schedules for the device.
Only trained personnel should perform repairs and maintenance on the device.
The recall covers all Olympus OER-Pro devices with the UDI: 04953170258589.
No, the recall does not require stopping use; it emphasizes proper maintenance and trained personnel for repairs.
Ensure you follow the safety warnings, maintenance schedules, and only use trained personnel for repairs.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-0873-2026 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-0873-2026 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.
