FDA Recall
Terminated
7245C, 7245C/E, 7245D Computer Digital Video System Product Usage: The 7245C, 7245C/E and 7245D are used to electronically record, display, transfer, and store digital video data of behavior related to swallowing in the pharyngeal area for medical and pedagogical applications.
Recall: Z-2742-2017
·
Initiated April 13, 2017
Recall
- Recall Number
- Z-2742-2017
- Event Number
- 77137
- Firm
- Pentax of America Inc
- FEI Number
- 1000080301
- Product Code
- GCW
- Status
- Terminated
- Root Cause
- Device Design
- Initiated
- April 13, 2017
- Terminated
- March 22, 2019
- Address
- 3 Paragon Dr, Montvale, NJ, 07645-1782
Description
7245C, 7245C/E, 7245D Computer Digital Video System Product Usage: The 7245C, 7245C/E and 7245D are used to electronically record, display, transfer, and store digital video data of behavior related to swallowing in the pharyngeal area for medical and pedagogical applications.
Reason
Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.
Action
Pentax notified their customers on 4/13/2017 via USPS.
Distribution
Worldwide Distribution - US Nationwide
Quantity
241 units in total