Incident · Recall
Stryker recalls Mako RIO over loss of system power mid-procedure
Stryker recalled the Mako RIO robotic-arm interactive orthopedic system because the system could lose power during a procedure. 20 units. Source: FDA Class 2 device recall Z-2741-2017, accessdata.fda.gov / openFDA enforcement.
Occurred 2017-06-07 · Stryker
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- Data documentation: /data
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Common questions
- What happened in Stryker recalls Mako RIO over loss of system power mid-procedure?
- Stryker recalled the Mako RIO robotic-arm interactive orthopedic system because the system could lose power during a procedure. 20 units. Source: FDA Class 2 device recall Z-2741-2017, accessdata.fda.gov / openFDA enforcement.
- When did this incident occur?
- The incident is recorded as occurring on June 7, 2017 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
- Who was involved in Stryker recalls Mako RIO over loss of system power mid-procedure?
- The incident is recorded as involving Stryker on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
- Has anyone responded to Stryker recalls Mako RIO over loss of system power mid-procedure?
- 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 Stryker recalls Mako RIO over loss of system power mid-procedure?
- This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Unreviewed · no sources on file · last reviewed 2026-06-27
Verification posture
Unreviewed
Low confidence
Review state
Stable
Last reviewed 2026-06-27
The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.
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Canonical ID 2c82347d-22ca-46f1-8cd8-c0a88d1db4fc