FDA Class II recall: SUNRISE instrument.
S3 · 25 Jul 2016 · Tecan
Record
| Company | Tecan |
| Industry | Medical robotics |
| Type(s) | recall |
| Date | 25 Jul 2016 (day precision) |
| Time of day | not documented |
| Location | no physical site (recall / fleet-wide / aggregate record) |
| Severity | (recall, enforcement, or fleet-wide fault) |
| Scale | SUNRISE instrument. |
| Confidence | high |
| Verified flag | Yes - 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
Publisher: openFDA enforcement · Retrieved: 2026-09-16
Supporting source rows (1)
| Date | Supporting source row | Publisher | Link |
|---|---|---|---|
| 25 Jul 2016 | FDA Class II recall: SUNRISE instrument. | openFDA enforcement | openFDA enforcement |
Tecan other incidents timeline
Medical robotics context
recall context
Tecan industry position
Related incidents
Other Tecan entries
- 29 May 2015 - FDA Class II recall: Infinite F500, in vitro diagnostic.
- 10 Nov 2014 - FDA Class III recall: Infinite 200PRO
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