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 · Investigated by FDA
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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: Verified · 1 source (1 primary) · last reviewed 2026-08-09
Verification posture
Verified
High confidence
Review state
Stable
Last reviewed 2026-08-09
Sources by quality tier
- 1
- primary-fda-database
- FDA database
The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.
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Canonical ID 2c82347d-22ca-46f1-8cd8-c0a88d1db4fc