Incident · Recall
Zimmer Biomet ROSA 2.5.8 recalled over a force-feedback sensor failure that can stop the arm from halting
A ROSA robot (software 2.5.8) was recalled because a force-feedback sensor failure could prevent the robotic arm from stopping as intended. 31 units. Source: FDA Class 2 device recall Z-0160-2018, accessdata.fda.gov / openFDA enforcement.
Occurred 2014-11-06 · Zimmer Biomet · Investigated by FDA
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Sources (1)
Common questions
What happened in Zimmer Biomet ROSA 2.5.8 recalled over a force-feedback sensor failure that can stop the arm from halting?
A ROSA robot (software 2.5.8) was recalled because a force-feedback sensor failure could prevent the robotic arm from stopping as intended. 31 units. Source: FDA Class 2 device recall Z-0160-2018, accessdata.fda.gov / openFDA enforcement.
When did this incident occur?
The incident is recorded as occurring on November 6, 2014 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 ROSA 2.5.8 recalled over a force-feedback sensor failure that can stop the arm from halting?
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 ROSA 2.5.8 recalled over a force-feedback sensor failure that can stop the arm from halting?
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 ROSA 2.5.8 recalled over a force-feedback sensor failure that can stop the arm from halting?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09
Verification posture
Verified
High confidence
Review state
Stable
Last reviewed 2026-08-09
Sources by quality tier
- 1
- primary-fda-database
- FDA database
The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.
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Canonical ID 5cec32b2-550e-41df-b9f4-0bc62d3d2f9e