FDA recall Z-2060-2018

Shimadzu Medical Systems · Class II · device

Product

Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device intended to be used for the radiography in the hospital with X-ray devices. This device is operated and used by the physicians and X-ray technologist. The object of this device is total patient population.

Reason for recall

When selecting serial radiography with a pulse rate of 7.5fps (including selecting a preset or changing the pulse rate using a temporary edit function) it was observed the indicated "irradiation time" on the X-ray Generator Console, as well as the "integral dose" on the external console of fluoroscopy, were reset to 0. There has been one report of this event.

Distribution

US Nationwide in the states of IL, WA, MI, TX, AZ, CA, LA, FL, SC, and NJ.

Key facts

Status
Terminated
Initiation date
2018-01-12
Report date
2018-06-20
Termination date
2022-02-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Torrance, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2060-2018