Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images of submucosal and peripheral organs of the upper gastrointestinal tract for observation, diagnosis and endoscopic treatment.
Recall
- Recall Number
- Z-0112-2014
- Event Number
- 66144
- Firm
- Fujinon Inc
- FEI Number
- 2431293
- Product Code
- FDS
- Status
- Terminated
- Root Cause
- Unknown/Undetermined by firm
- Initiated
- July 31, 2013
- Posted
- October 30, 2013
- Terminated
- March 4, 2014
- Address
- 10 Highpoint Dr, Wayne, NJ, 07470
Description
Fujinon/Fujifilm Ultrasonic Endoscope Intended to provide ultrasonic images of submucosal and peripheral organs of the upper gastrointestinal tract for observation, diagnosis and endoscopic treatment.
A limited number of endoscopes were shipped to FMSU-ESD with a manufacturing defect which included missing set screws used to more securely attach the Forceps Inlet (biopsy inlet port) to the endoscope.
The firm, FUJIFILM Medical Systems, USA, Inc. (FMSU-ESD) sent an "URGENT-MEDICAL DEVICE CORRECTION (UMDC)" and Customer Acknowledgement forms dated July 31, 2013 to their customers. The letter described the issue with the affected product; instructed customers on how to identify affected units; instructed customers to immediately cease use of the affected units; return affected units to FMSU-ESD for repairs and quality control inspection; and complete and return the attached "Customers Acknowledgement" form to FMSU-ESD, Attn: Regulatory Compliance, via fax to (973) 686-2616 or email: [email protected]. If you have any questions regarding this notice, please do not hesitate to contact Director, Quality and Regulatory Compliance, at (973) 686-2636 or by email: [email protected].
Worldwide distribution: US (nationwide) including states of: NJ, PA and VA; and country of Canada.
12 Units