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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 Mako SmartRobotics at Global · Stryker · Global · Surgical robots · Investigated by FDA

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Sources (2)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?start_search=1&firmlegalnam=Stryker&productdescriptiontxt=Mako&postdatefrom=01/01/2017&postdateto=12/31/2026&PAGENUM=100
  2. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=156493

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.
What robot was involved in Stryker recalls Mako RIO over loss of system power mid-procedure?
Stryker Mako SmartRobotics by Stryker is the recorded robot involved in this incident at Global.
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 · 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.

Methodology surface for Stryker recalls Mako RIO over loss of system power mid-procedure.

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Canonical ID 2c82347d-22ca-46f1-8cd8-c0a88d1db4fc