---
title: "Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 25892... — FDA record Z-2047-2026 | Is It on Recall"
description: "Potential for mislabeled syringe produced by the i.v.STATION device."
url: https://isitonrecall.com/recall/fda-device-z-2047-2026-rolls-of-label-stock-used-with-the-omnicell-i-v-station-1-part-number-258920028-label-sterile-ivstat/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE ... — FDA record Z-2047-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 25, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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 compounding of IV medications, which also applies labels to compounded preparations for identification and traceability.
- **Reason**: Potential for mislabeled syringe produced by the i.v.STATION device.
- **Classification**: Class I
- **Recalling firm**: Omnicell, Inc.
- **Quantity**: 220 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2047-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2047-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 1. Part Number 258920028, Lot Number: QN 200023473. 2. Part Number 258900029, Lot Number: QN 200023474. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Distribution in Alabama, Maryland and Pennsylvania.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alabama](https://isitonrecall.com/state/alabama/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)

## Dates in the source

- **Report date**: May 20, 2026
- **Recall initiation date**: Mar 25, 2026
- **Center classification date**: May 13, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2047-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [OmniCell, Inc. records](https://isitonrecall.com/brand/omnicell-inc/)