FDAClass IMay 20, 2026

Rolls of label stock used with the Omnicell recall: Labeling Error

Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number…

Why was Rolls of label stock used with the Omnicell recalled?

Potential for mislabeled syringe produced by the i.v.STATION device.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

1. Part Number 258920028, Lot Number: QN 200023473. 2. Part Number 258900029, Lot Number: QN 200023474.

Product
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number…
Recalling firm
Omnicell, Inc.
Quantity
220 units
Distribution
US Distribution in Alabama, Maryland and Pennsylvania.
Recall date
May 20, 2026
Classification
Class I
Status
Ongoing
Agency
FDA (device)
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