_Incident · Recall_

# Zimmer Biomet recalls ROSA Brain 3.0 over insufficient washers allowing telescopic-arm movement

Canonical ID: `360d465e-1935-44fd-89b4-b2f764491873`

- **Occurred:** 2016-05-27
- **Kind:** `recall`
- **Status (derived):** active
- **Company:** [Zimmer Biomet](/companies/zimmer-biomet.md) (id: `bf360924-7c7c-4b17-8fcf-8abf5950c0ff`)

Zimmer Biomet recalled the ROSA Brain 3.0 because insufficient washers in the telescopic arm could allow some unintended movement. 3 units. Source: FDA Class 2 device recall Z-0105-2018, openFDA enforcement / accessdata.fda.gov.

## Sources (0)

_No sources on file._

## Common questions

### What happened in Zimmer Biomet recalls ROSA Brain 3.0 over insufficient washers allowing telescopic-arm movement?

Zimmer Biomet recalled the ROSA Brain 3.0 because insufficient washers in the telescopic arm could allow some unintended movement. 3 units. Source: FDA Class 2 device recall Z-0105-2018, openFDA enforcement / accessdata.fda.gov.

### When did this incident occur?

The incident is recorded as occurring on May 27, 2016 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 Brain 3.0 over insufficient washers allowing telescopic-arm movement?

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 Brain 3.0 over insufficient washers allowing telescopic-arm movement?

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 Brain 3.0 over insufficient washers allowing telescopic-arm movement?

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


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