Products: pharmacy-automation. Risk band: Elevated RobotRisk index 26.7/100 (incidents/exposure, time-weighted) · 96th percentile of 162 medical robotics companies.
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. This one entry produces an index of 26.9 and places the company at the 95.7th percentile within medical-robotics, an elevated band. 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.
| Sev | Date | Type | Location | Incident | Source |
|---|---|---|---|---|---|
| S4 | 03/25 2026 |
recall | — | FDA Class I recall: Rolls of label stock used with the Omnicell i.v.Station. · Rolls of label stock used with the Omn… | openFDA enforcement |