Device recall

Z-2626-2017: ROTH MOBELI Grab Handles used with EOS System: MOBELI Stabi Vario Grab Handle…

FDA device recall · Class II · EOS Imaging

Key facts

Recall number (Z-number) Z-2626-2017
Recall event 77424
Product ROTH MOBELI Grab Handles used with EOS System: MOBELI Stabi Vario Grab Handle, ROTH Catalogue Number 14002 96 S, EOS Imaging Catalogue Number 9000111773; and MOBELI Dual Grip Grab Handle, ROTH Catalogue Number 14002 25 S, EOS Imaging Catalogue Number 9000111774.
Product code IKX
Recalling firm EOS Imaging
Recall class Class II
Status Terminated
Termination date Oct 9, 2018
FEI number 3006165260

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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

Browse all FDA device recalls (products)