_Incident · Recall_

# Zimmer Biomet recalls ROSA Surgical Device 2.5.8 over observed device instability

Canonical ID: `595f469f-e2a0-4559-80b2-34ad1080a47b`

- **Occurred:** 2013-02-05
- **Kind:** `recall`
- **Status (derived):** active
- **Company:** [Zimmer Biomet](/companies/zimmer-biomet.md) (id: `bf360924-7c7c-4b17-8fcf-8abf5950c0ff`)

Zimmer Biomet recalled the ROSA Surgical Device 2.5.8 over observed device instability. 53 units. Source: FDA Class 2 device recall Z-0099-2018, openFDA enforcement / accessdata.fda.gov.

## Sources (0)

_No sources on file._

## Common questions

### What happened in Zimmer Biomet recalls ROSA Surgical Device 2.5.8 over observed device instability?

Zimmer Biomet recalled the ROSA Surgical Device 2.5.8 over observed device instability. 53 units. Source: FDA Class 2 device recall Z-0099-2018, openFDA enforcement / accessdata.fda.gov.

### When did this incident occur?

The incident is recorded as occurring on February 5, 2013 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.

### Who was involved in Zimmer Biomet recalls ROSA Surgical Device 2.5.8 over observed device instability?

The incident is recorded as involving Zimmer Biomet on the DEPLOY registry. No specific robot model is linked to this incident in the registry.

### Has anyone responded to Zimmer Biomet recalls ROSA Surgical Device 2.5.8 over observed device instability?

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 Zimmer Biomet recalls ROSA Surgical Device 2.5.8 over observed device instability?

This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.


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