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FDA Class II recall: Trexo Device

S3 · 31 May 2023 · Trexo Robotics

Record

CompanyTrexo Robotics
IndustryMedical robotics
Type(s)recall
Date31 May 2023 (day precision)
Time of daynot documented
Locationno physical site (recall / fleet-wide / aggregate record)
Severity (recall, enforcement, or fleet-wide fault)
ScaleTrexo Device
Confidencehigh
Verified flagYes - independently re-checked against the cited source

Summary

FDA enforcement record (Class II, recall Z-2236-2023): Electrical issues that could potentially render the device non-functional, give off electromagnetic influence to surrounding equipment, and risk of burns when in use.

Primary source

openFDA enforcement

Publisher: openFDA enforcement · Retrieved: 2026-09-16

Supporting source rows (1)
DateSupporting source rowPublisherLink
31 May 2023 FDA Class II recall: Trexo Device openFDA enforcement openFDA enforcement

Medical robotics context

recall context

Trexo Robotics industry position

Related incidents

Other Trexo Robotics entries

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