Olympus recalls GF-UC140P-AL5 ultrasonic gastrovideoscopes due to infection risk when reprocessed with OER-Pro systems. All units with serial numbers sold in the US are affected.
GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the OER-Pro and presents an infection control risk to patients
Olympus is recalling its GF-UC140P-AL5 ultrasonic gastrovideoscopes because they are no longer compatible with the OER-Pro reprocessing system, creating an infection risk for patients. This affects all units sold in the US with serial numbers listed in the recall.
The GF-UC140P-AL5 model is no longer compatible with the OER-Pro reprocessing system. This means the device cannot be safely cleaned and sterilized using the standard method, potentially leading to infections for patients.
Healthcare professionals using the device for endoscopic ultrasound imaging in the US are affected. Patients receiving procedures with this device may be at risk of infection if the device isn't properly reprocessed.
Check the serial number on the device. All units sold in the US with the model GF-UC140P-AL5 are affected. The product has a GTIN of 04953170356322.
Verify if your device is compatible with the OER-Pro reprocessing system by checking the serial number.
The device is safe for use but must be reprocessed correctly to avoid infection risks. Incompatible units should not be used with the OER-Pro system.
All units with the model GF-UC140P-AL5 sold in the US are affected. Check the serial number on the device.
The recall does not specify a remedy, so contact Olympus directly for guidance on safe reprocessing or disposal.
We’ve drafted a message you can send Olympus to request your refund or repair — edit it as you like.
Subject: Recall Z-1034-2022 — Olympus Olympus Hello, I own a Olympus that is covered by recall Z-1034-2022 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.
