FDAJuly 12, 2022device

AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis, Hemo LOW 6634633; AXIOM Sensis, Combo 32 6634641; AXIOM Sensis, EP 129 6634658; Sensis 10764561; Sensis Vibe Combo 11007642; Sensis recording system is intended to be used as a di...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g., at the patient table), In the event the mounting position deviates from the default position, the following are possible: Patient touching the Signal Input Box may result in a touch leakage current to the patient; Spillage of liquid entering the Signal Input Box

What to do

FDA enforcement status: Terminated

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

0405686901013704056869010205

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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