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  5. Automated Compounding System Recall: Omnicell Removes Syringe Labels Used with the i.v.STATION Automated Compounding System
  1. Medical Device Recalls and Early Alerts

Automated Compounding System Recall: Omnicell Removes Syringe Labels Used with the i.v.STATION Automated Compounding System

This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. The affected products and recommendations for what to do with the devices below have not changed.

Affected Product

The FDA is aware that Omnicell has issued a letter to affected customers recommending certain syringe labels used with the i.v.STATION automated compounding system be removed from where they are used or sold.

Affected devices:

  • IVSTATION SYRINGE sterile label (40MMX40MM) - part number 258920028
  • IVSTATION SYRINGE sterile label (20MMX40MM) - part number 258920029  

These labels come individually wrapped in a plastic overwrap with a white backing.

What to Do

Do not use affected labels. Verify accuracy of labels on filled products.

On April 10, Omnicell sent all affected customers a letter recommending the following actions:

  • Do not use labels affected by this recall. If you or your staff locate any affected labels, immediately segregate and contact Omnicell Technical Support.
  • Revert to the use of previously ordered non-sterile syringe labels with yellow backing (part number HR060027 and HR060071).
  • Engage in vigilant pharmacist verification practices to verify the accuracy of labels per your existing review process.
  • Share this information with all those who need to be aware within your organization.

Reason for Recall

Omnicell received a report of mislabeling that could affect sterile syringe labels produced using i.v.STATION. Omnicell identified inconsistent label detection behavior across i.v.STATION printers when using the sterile labels affected by this recall.

Inconsistent label detection could result in unlabeled or mislabeled syringe preparations after compounding completion where the above identified sterile labels are utilized.

As of April 10, Omnicell has reported no serious injuries or deaths associated with this issue.

Device Use

i.v.STATION is an automation device that limits the need to manually handle vials, solutions, IV bags, and syringes during the preparation and compounding of IV medications, while also minimizing cross-contamination between drugs.  As part of the device's automation, it applies labels to compounded preparations for identification and traceability.

Contact Information

Customers in the U.S. with adverse reactions, quality problems, or questions about this issue should contact Omnicell at 817-3574904.

Additional FDA Resources

  1. FDA Enforcement Report
  2. CDRH Medical Device Recall Database 

How do I report a problem?  

Health care professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program.

Timeline of Communication Updates

DateActions
05/21/2026The FDA updated this communication to inform the public that this issue has been classified as a Class I Recall.
04/24/2026The FDA issued an Early Alert communication to notify the public of a potentially high-risk device issue.

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