Update: Import Alert for Certain Olympus Medical Devices Manufactured in Japan – Letter to Health Care Providers

October 20, 2026

The U.S. Food and Drug Administration (FDA) is alerting health care providers about an import alert for certain medical devices manufactured in Japan by Olympus Medical Systems Corporation (Olympus) and its subsidiaries. Despite extensive and ongoing efforts to address compliance issues, the FDA continues to have concerns related to outstanding Quality System regulation violations by Olympus. Therefore, the FDA has issued an import alert to prevent future shipments of certain devices from entering the United States, including specific models of: 

• Ureterorenoscopes, which are used to perform various diagnostic and therapeutic procedures within the urinary tract,
• Bronchoscopes, which are used to perform various diagnostic and therapeutic procedures in the respiratory tract, 
• Laparoscopes, which are used to perform various diagnostic and therapeutic procedures in the abdomen and pelvis,  
• Automated endoscope reprocessors, which are used to reprocess various endoscopes,
• Ingestible telemetric gastrointestinal capsule imaging systems, which are used for visualization of the small bowel mucosa, and
• Enteroscopes, which are used to provide visualization and perform procedures within the small intestine.

Recommendations for Health Care Providers

The FDA recommends that health care providers:

• Be aware of the FDA import alert for certain medical devices manufactured in Japan by Olympus Medical Systems Corporation (Olympus), under which the devices will be refused entry into the U.S.:
• Refer to the table below for model numbers and Unique Device Identifiers (UDI) for the devices included in the import alert.
  • Be aware that the import alert does not apply to related products (such as replacement parts, connectors, or single use consumables) used with the devices subject to import alert.  
• If devices subject to the import alert are currently in use, users may continue using them if they are not experiencing any problems with the devices.
  • Follow the labeling and reprocessing instructions to properly clean and reprocess the devices, including accessory components.
  • Do not use damaged devices or those that have failed a leak test, as they could be a potential source of contamination.
  • Develop schedules for routine inspection and periodic maintenance in accordance with manufacturer’s instructions.
• Be aware that some devices under this import alert may have been recalled. If devices subject to the import alert were recalled, users should follow the firm’s recall customer notification letter, which should provide specific product instructions identified by the firm.
• Discuss the benefits and risks associated with procedures involving these devices with your patients. The FDA does not recommend that procedures be canceled or delayed without discussion of the benefits and risks between the health care provider and patient.
• Complete prompt reporting of adverse events to help the FDA identify and better understand the risks associated with these devices.

Background

The FDA has issued warning letters and import alerts regarding current good manufacturing practice (CGMP) requirements and various reporting requirements, including recalls that the FDA identified as the most serious type of recall.

FDA Actions

The FDA has taken several actions related to quality system requirements and compliance concerns with Olympus.  

The FDA monitors corrective actions related to ongoing device quality violations. The FDA takes seriously its role in ensuring that medical devices are safe and effective.

The FDA will continue to keep health care providers and the public informed if new or additional information becomes available.

Unique Device Identifier

The FDA established the unique device identification system (UDI) to adequately identify medical devices sold in the United States from manufacturing through distribution to patient use.

List of Olympus Devices Subject to Import Alert

Timeline of Communication Updates

A timeline and summary of the FDA’s previous communications related to this issue are provided below.

Reporting Problems to the FDA

The FDA encourages health care providers to report any adverse events or suspected adverse events experienced with medical devices manufactured by Olympus:

By promptly reporting adverse events, you can help the FDA identify and better understand the risks associated with medical devices.

Contact Information

If you have questions about this letter, contact the Office of Industry and Consumer Education (OICE).

Additional Resources