EVIS EXERA III Bronchovideoscope
FDA Recall Z-1559-2022 · Posted None
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Recalling FirmAizu Olympus Co., Ltd.
Recall StatusTerminated
Product CodeEOQ
Date Initiated2022-07-20
Date Terminated2025-01-22
Reason for Recall
The recalled unit was utilized in a veterinary endoscopy procedure in advance of being assigned to healthcare facilities as a loaner.
Firm Action
An Urgent Field Safety Notice was distributed by the recalling firm on 07/20/2022 notifying consignees that a bronchoscope utilized in a veterinary endoscopy procedure was subsequently distributed as a service loaner in error. The device was utilized in a single procedure on a cat. Actions to be taken by customers include evaluating the situation according to hospital procedure to determine if patient notification or follow up may be required, review patient records and report any potentially adverse events to Olympus and FDA and acknowledge receipt of the recall notification by email or through the Olympus recall portal at https://olympusamerica.com/recall. Customers with any questions may contact Cynthia Ow by phone at (647)999-3203 or by email at [email protected]. Customers reporting complaints associated with this recall event are to call Olympus at 1-800-848-9024, option 1.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states of FL, IL, NC, PA & TX.
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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