Omnicell, Inc. 2026-05-20 Health critical FDA
Health · FDA · Recall #FDA-Z-2047-2026
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028,… Recall
Issued May 20, 2026 · Omnicell, Inc.
In May 2026, Omnicell, Inc. recalled the Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028,…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for mislabeled syringe produced by the i.v.STATION device.
What you should do
- 1 Stop using Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Omnicell, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Omnicell, Inc.
- Category
- Health
- Recall date
- May 20, 2026
- Units affected
- Not reported
- Sold at
- US Distribution in Alabama, Maryland and Pennsylvania.
- Recall number
- FDA-Z-2047-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Omnicell, Inc. has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.