Philips Healthcare Inc.: Medical Device Recall in 2013 - (Recall #: Z-0702-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general use

Product Classification:

Class II

Date Initiated: December 13, 2012

Date Posted: February 6, 2013

Recall Number: Z-0702-2013

Event ID: 63868

Reason for Recall:

Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not be displayed "at the fluoroscopist's working position" as per 21 CFR 1003.21

Status: Terminated

Product Quantity: 16 units

Code Information:

Serial Numbers: 10110770 11030805 11070848 11070845 11070849 11030806 11090864 11110900 12020982 114087 12030999 12061020 12041003 12061014 12061018 12081040 :

Distribution Pattern:

US Nationwide Distribution including the states of AL, CA, CO, CT, IL, MD, MI, MO, NY, OH, PA

Voluntary or Mandated:

Voluntary: Firm initiated