Omnicell
Products: pharmacy-automation. Risk band: Elevated RobotRisk index 44.5/100 (severity- and time-weighted incidents) · ranked 4 of 25 among Medical robotics companies with incidents (173 tracked).
Analyst brief
Omnicell's record consists of a single entry, an FDA Class I recall of label stock used with the i.v.Station device, carrying severity 4. Omnicell's index of 44.6 ranks 4 of 25 companies in Medical robotics with incident history. The record is regulatory in nature, originating from an FDA recall classification rather than press incident reporting. As a single-event record, it reflects one classified regulatory action rather than a recurring pattern, though the Class I designation denotes the highest FDA severity tier for recalls.
Risk index
Incident timeline
Comparisons over time
Per-type breakdown
| Incident type | Unique incidents | Share |
|---|---|---|
| recall | 1 | 100% |
Unique incident list
1 unique incident on file for this company.
| Sev | Date | Type | Location | Incident | Source |
|---|---|---|---|---|---|
| S4 | 25 Mar 2026 | recall | — | FDA Class I recall: Rolls of label stock used with the Omnicell i.v.Station. · Rolls of label stock used with the Omnicell i.v.Station. | openFDA enforcement |
S4 25 Mar 2026 · recall · FDA Class I recall: Rolls of label stock used with the Omnicell i.v.Station.
| Sev | Date | Supporting source row | Source |
|---|---|---|---|
| S4 | 25 Mar 2026 | FDA Class I recall: Rolls of label stock used with the Omnicell i.v.Station. | openFDA enforcement |
Similar companies
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