PlainRecalls
FDA Devices Moderate Class II Terminated

Video Cystoscope models ECY-1570 and ECY-1570K

Reported: February 21, 2018 Initiated: July 13, 2017 #Z-0615-2018

Product Description

Video Cystoscope models ECY-1570 and ECY-1570K

Reason for Recall

The video cytoscopes lack 510(k) premarket notification clearance.

Details

Recalling Firm
Pentax of America Inc
Units Affected
24
Distribution
Distributed in 8 states: CA, IL, MD, MI, ND, NH, NY, SD, and Guam.
Location
Montvale, NJ

Frequently Asked Questions

What product was recalled?
Video Cystoscope models ECY-1570 and ECY-1570K. Recalled by Pentax of America Inc. Units affected: 24.
Why was this product recalled?
The video cytoscopes lack 510(k) premarket notification clearance.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 21, 2018. Severity: Moderate. Recall number: Z-0615-2018.