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RobotRiskTecan › 25 Jul 2016

FDA Class II recall: SUNRISE instrument.

S3 · 25 Jul 2016 · Tecan

Record

CompanyTecan
IndustryMedical robotics
Type(s)recall
Date25 Jul 2016 (day precision)
Time of daynot documented
Locationno physical site (recall / fleet-wide / aggregate record)
Severity (recall, enforcement, or fleet-wide fault)
ScaleSUNRISE instrument.
Confidencehigh
Verified flagYes - independently re-checked against the cited source

Summary

FDA enforcement record (Class II, recall Z-2661-2016): The batteries have the potential to overheating, melt or char.

Primary source

openFDA enforcement

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

Supporting source rows (1)
DateSupporting source rowPublisherLink
25 Jul 2016 FDA Class II recall: SUNRISE instrument. openFDA enforcement openFDA enforcement

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