Incident · Recall
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.
Occurred 2013-02-05 · Zimmer Biomet
Machine-readable surfaces
- Markdown mirror: /incidents/zimmer-rosa-258-device-instability-recall-2018.md
- JSON-LD: embedded in this page’s head
- REST API: /v1/incidents/595f469f-e2a0-4559-80b2-34ad1080a47b
- Data documentation: /data
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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.
Methodology: Unreviewed · no sources on file · last reviewed 2026-06-27
Verification posture
Unreviewed
Low confidence
Review state
Stable
Last reviewed 2026-06-27
The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.
Methodology surface for Zimmer Biomet recalls ROSA Surgical Device 2.5.8 over observed device instability.Deploy Watch
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Canonical ID 595f469f-e2a0-4559-80b2-34ad1080a47b