fda_recall · device_recall · critical
Omnicell, Inc. — Class I recall: Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258…
- Event date
- 2026-05-20 00:00:00Z
- Observed
- 2026-07-09 22:52:28Z
- Source ID
- Z-2047-2026
- Payload hash
- 33ba554326d3f0c07428db9e…
Summary
Potential for mislabeled syringe produced by the i.v.STATION device. Status: Ongoing.
Entities
Informational only. Not legal, financial, or medical advice.