RecallRadar

FDA Device recall Z-2626-2017

ROTH MOBELI Grab Handles used with EOS System: MOBELI Stabi Vario Grab Handle, ROTH Catalogue Number 14002 96 S, EOS Imaging Catalogue Numb…

On 2017-07-05 the FDA classified a Class II recall of ROTH MOBELI Grab Handles used with EOS System: MOBELI Stabi Vario Grab Handle, ROTH Catalogue Number 14002 96 S, EOS Imaging Catalogue Numb… by Eos Imaging, citing ROTH MOBELI grab handles could detach and patient could fall if the EOS system operator does not follow instructions. Before each use, the operator must examine the vacuum safety….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2626-2017
ClassificationClass II
Statusterminated
Initiated2017-05-30
Published2017-07-05
Last updated2026-09-13 11:54 UTC
CompanyEos Imaging
DistributionAL, MA, MI, MN, PA, TX, WA

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.

Reason

ROTH MOBELI grab handles could detach and patient could fall if the EOS system operator does not follow instructions. Before each use, the operator must examine the vacuum safety indicator to check the vacuum is monitored and sufficient and the grab handle correctly attached. Do not use grab handles to help patient up. The handles are only for stabilizing the patients hand or arm in the EOS cabin.

Identifiers

code_infoROTH Catalogue Numbers 14002 96 S and 14002 25 S only,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2626-2017%22

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