Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0067-2026Class I

Oes Bronchofiberscope Olympus Bf Type Xt40

OLYMPUS Corporation of the Americas / initiated 2025-09-11 / Open, Classified / root cause: design

Olympus Corporation of the Americas began a recall of OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 on . FDA classified it as Class I and gives the reason as "Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment". As of , the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number
Z-0067-2026
Classification
Class I
Status
Open, Classified
Initiated
Posted
Recalling firm
OLYMPUS Corporation of the Americas
Product
Oes Bronchofiberscope Olympus Bf Type Xt40
Product code
EOQ Bronchoscope (Flexible Or Rigid)
Reason for recall
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Root cause tag
design
FDA root cause
Device Design
Action
An URGENT Medical Device Correction notification dated 9/11/25 was mailed to consignees to notify them of this recall action. Consignees are asked to carefully read the recall notification and identify any affected devices in their inventory. Consignees are to ensure all personnel are knowledgeable and aware of the updated IFU. Consignees are to acknowledge receipt of the recall notification through Olympus' web portal at https://olympusamerica.com/recall. Forward the provided recall notification if product was further distributed. Consignees with any questions can contact Cynthia Ow by phone at 647-999-3203 or by email at [email protected].
Quantity in commerce
116 units US; 705 units OUS
Distribution
US Nationwide Distribution.
Product codes and lots
Model No. BF-XT40; UDI: n/a; All Serial No.

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-0067-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-0045-2026Class IOngoingVoluntary: Firm initiated
Z-0046-2026Class IOngoingVoluntary: Firm initiated
Z-0047-2026Class IOngoingVoluntary: Firm initiated
Z-0048-2026Class IOngoingVoluntary: Firm initiated
Z-0049-2026Class IOngoingVoluntary: Firm initiated
Z-0050-2026Class IOngoingVoluntary: Firm initiated
Z-0051-2026Class IOngoingVoluntary: Firm initiated
Z-0052-2026Class IOngoingVoluntary: Firm initiated
Z-0053-2026Class IOngoingVoluntary: Firm initiated
Z-0054-2026Class IOngoingVoluntary: Firm initiated
Z-0055-2026Class IOngoingVoluntary: Firm initiated
Z-0056-2026Class IOngoingVoluntary: Firm initiated
Z-0057-2026Class IOngoingVoluntary: Firm initiated
Z-0058-2026Class IOngoingVoluntary: Firm initiated
Z-0059-2026Class IOngoingVoluntary: Firm initiated
Z-0060-2026Class IOngoingVoluntary: Firm initiated
Z-0061-2026Class IOngoingVoluntary: Firm initiated
Z-0062-2026Class IOngoingVoluntary: Firm initiated
Z-0063-2026Class IOngoingVoluntary: Firm initiated
Z-0064-2026Class IOngoingVoluntary: Firm initiated
Z-0065-2026Class IOngoingVoluntary: Firm initiated
Z-0066-2026Class IOngoingVoluntary: Firm initiated
Z-0067-2026Class IOngoingVoluntary: Firm initiated