Drug recall
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION…
FDA recall event 98717 · Class I · Omnicell, Inc.
Key facts
| Event ID | 98717 |
|---|---|
| Recall numbers | Z-2047-2026 |
| Recalling firm | Omnicell, Inc. |
| Product type | Devices |
| Products | Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number 258900029, LABEL, STERILE, IVSTATION SYRINGE… |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for mislabeled syringe produced by the i.v.STATION device. |
| Initiation date | Mar 25, 2026 |
| Report date | May 20, 2026 |
| City | Cranberry Township |
| State | PA |
| Country | United States |
| FEI number | 3007880912 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: