Device recall

Z-0571-2013: SpineSix consists of a motorized treatment table that is controlled by an…

FDA device recall · Class II · BioMotion Medical Systems, LLC

Key facts

Recall number (Z-number) Z-0571-2013
Recall event 63788
Product SpineSix consists of a motorized treatment table that is controlled by an integral computer. The system is operated by means of 12-inch Color LCD touch screen that displays treatment time, positioning and magnitude and direction of motion. There are eight fully customizable Patient Protocol settings…
Product code BXB
Recalling firm BioMotion Medical Systems, LLC
Recall class Class II
Status Terminated
Termination date Nov 5, 2013
FEI number 3009896513

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 1–9 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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