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Zimmer ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE)

An FDA MAUDE injury report describes a Zimmer ROSA Recon case in which reaming resulted in an oblong hole due to hard bone, and the surgeon grafted the defect. Source: FDA MAUDE MDR key 24316286, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.

Occurred 2024-06-24 · Zimmer Biomet · Investigated by FDA

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Incident records on DEPLOY are compiled from public sources (regulatory filings, news reports, and operator disclosures) and reflect what has been reported and tracked to date. They are not legal findings, determinations of fault, or safety ratings, and may be updated as new information is verified. See the sources below for the underlying references.
Track Zimmer ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE)

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Sources (3)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/search.cfm
  2. https://www.zimmerbiomet.com/
  3. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=24316286&pc=OLO

Common questions

What happened in Zimmer ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE)?
An FDA MAUDE injury report describes a Zimmer ROSA Recon case in which reaming resulted in an oblong hole due to hard bone, and the surgeon grafted the defect. Source: FDA MAUDE MDR key 24316286, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.
When did this incident occur?
The incident is recorded as occurring on June 24, 2024 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in Zimmer ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE)?
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 ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE)?
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 ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE)?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 3 sources (2 primary) · last reviewed 2026-08-09

Verification posture

Verified

High confidence

Review state

Stable

Last reviewed 2026-08-09

Sources by quality tier

2
primary-fda-database
FDA database
1
unclassified
Unclassified source

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for Zimmer ROSA Recon: reaming produced an oblong hole requiring a bone graft (FDA MAUDE).

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Canonical ID 8857ebf9-c75a-4800-b423-bea3a37676fa