Device recall
Z-2047-2026: Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number…
FDA device recall · Class I · Omnicell, Inc.
Key facts
| Recall number (Z-number) | Z-2047-2026 |
|---|---|
| Recall event | 98717 |
| Product | 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 (20MMX40MM). Model/Catalog Number: IVS-RBT-001. i.v.STATION is an automation device used for preparation and… |
| Product code | NEP |
| Recalling firm | Omnicell, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3007880912 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database