Device recall

Z-1564-2008: GE Healthcare Precision RXi Digital Remote X-Ray Imaging R&F System. It is a…

FDA device recall · Class II · GE Healthcare

Key facts

Recall number (Z-number) Z-1564-2008
Recall event 46807
Product GE Healthcare Precision RXi Digital Remote X-Ray Imaging R&F System. It is a remote R&F system consisting of a tilting table with integrated spot film device, 65 or 89 kW pulsing generator and high heat capacity X-Ray tube. The system can be configured to meet a wide variety of digital record and…
Product code JAA
Recalling firm GE Healthcare
Recall class Class II
Status Terminated
Termination date Aug 9, 2012
510(k) numbers K041605
FEI number 2126677

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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