Incident · Malfunction
Medtronic Hugo RAS: failure to calibrate with the application program freezing or failing to launch (FDA MAUDE)
An FDA MAUDE malfunction report describes a Medtronic Hugo RAS failure to calibrate during which the application program froze or failed to launch. Source: FDA MAUDE MDR key 25333336, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.
Occurred 2026-05-21 · Medtronic · Investigated by FDA
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Sources (2)
Common questions
What happened in Medtronic Hugo RAS: failure to calibrate with the application program freezing or failing to launch (FDA MAUDE)?
An FDA MAUDE malfunction report describes a Medtronic Hugo RAS failure to calibrate during which the application program froze or failed to launch. Source: FDA MAUDE MDR key 25333336, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.
When did this incident occur?
The incident is recorded as occurring on May 21, 2026 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in Medtronic Hugo RAS: failure to calibrate with the application program freezing or failing to launch (FDA MAUDE)?
The incident is recorded as involving Medtronic on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to Medtronic Hugo RAS: failure to calibrate with the application program freezing or failing to launch (FDA MAUDE)?
No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.
What is the current status of Medtronic Hugo RAS: failure to calibrate with the application program freezing or failing to launch (FDA MAUDE)?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 2 sources (2 primary) · last reviewed 2026-08-09
Verification posture
Verified
High confidence
Review state
Stable
Last reviewed 2026-08-09
Sources by quality tier
- 2
- primary-fda-database
- FDA database
The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.
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Canonical ID 2c68da23-4ec5-4fe7-9041-e7d61af226ae