Omnicell recalls label stock for i.v.Station devices that may cause mislabeled syringes. Affected parts include specific part numbers and lot numbers. Consumers should check their devices for the listed identifiers.
Potential for mislabeled syringe produced by the i.v.STATION device.
Omnicell is recalling rolls of label stock used with their i.v.Station devices because they could be mislabeled, leading to incorrect syringe identification. This poses a risk of using the wrong syringes during medication preparation.
The label stock could produce syringes with incorrect labels, which might lead to using the wrong syringes during medication preparation. This could cause errors in medication administration if the labels are not properly identified.
Healthcare professionals using Omnicell i.v.Station devices with the recalled label stock are most at risk. Patients receiving medications compounded with these devices may also be affected if the labels are incorrect.
Check for part numbers 258920028 (40mm x 40mm) or 258900029 (20mm x 40mm) on the label stock rolls. The lot numbers QN 200023473 and QN 200023474 are also associated with these parts.
Inspect your i.v.Station label stock rolls for part numbers 258920028 or 258900029 and lot numbers QN 200023473 or QN 200023474.
The recalled label stock has part numbers 258920028 (40mm x 40mm) and 258900029 (20mm x 40mm).
Check for part numbers 258920028 or 258900029 and lot numbers QN 200023473 or QN 200023474 on the label stock rolls.
No, the recall is for the label stock, not the i.v.Station device itself. You can continue using the device if you have the correct label stock.
We’ve drafted a message you can send Omnicell to request your refund or repair — edit it as you like.
Subject: Recall Z-2047-2026 — Omnicell Omnicell Hello, I own a Omnicell that is covered by recall Z-2047-2026 from Omnicell. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
