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FUJIFILM

FUJIFILM CORPORATION · Model SU-1 FV667A · UDI-DI 04547410332377

ITX IYN IYO FDS Prescription

510(k) clearances

4,015

Adverse events (23 deaths)

147

Recalls

397

Facilities

Description

The Fujifilm ultrasonic processors SU-1 is intended to be used in combination with Fujifilm ultrasonic endoscope, video processor, light source, monitor, recorder, and various peripheral devices. The product is intended to provide ultrasonic images of the trachea, bronchial tree and surrounding organs, or submucosal and peripheral organs of the upper gastrointestinal tract for observation, recording and to aid in diagnosis during endoscopic evaluation.

Recalls

Date	Firm	Reason
2025-11-17	Sheathing Technologies Inc	Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
2025-09-05	Philips Ultrasound, Inc	To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.