PCF-H190L, EVIS EXERA III COLONOVIDEOSCOPE
FDA Recall Z-0419-2024 · Posted 2023-11-29
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Recalling FirmAizu Olympus Co., Ltd.
Recall StatusOpen, Classified
Product CodeFDF
Date Initiated2023-10-16
Product Quantity24 incorrectly repaired units
Reason for Recall
Specific devices may have an improperly repaired light guide connector due to missing adhesive to secure the suction channel mouthpiece to the scope connector. Issue may result in loss of image, decreased suction, or impact the ability to effectively reprocess the device. This in turn may lead to unanticipated delay to treatment, or patient exposure to contaminated material and subsequent infection.
Firm Action
On October 16, 2023, the firm notified affected customers through URGENT MEDICAL DEVICE REMOVAL letters. Customers were instructed to inspect their inventory and identify affected devices. Affected devices should be quarantined and not used.
Olympus Customer Solutions will contact customers by phone and email to arrange the return and repair of the affected product.
If you require additional information, please do not hesitate to contact Olympus at 647-999-3203 or [email protected].
Root Cause
Process control
Distribution Pattern
Domestic distribution to FL, KY, MA, NJ, NY, and PA
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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