_Incident · Recall_

# Stryker recalls Mako RIO over loss of system power mid-procedure

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

- **Occurred:** 2017-06-07
- **Kind:** `recall`
- **Status (derived):** active
- **Company:** [Stryker](/companies/stryker.md) (id: `661fbd42-9fcb-4d47-8a74-7a23d161d57b`)

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.

## Sources (0)

_No sources on file._

## 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.


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