United StatesRolls of sterile label stock used with the Omnicell i.v.STATION (Model/Catalog IVS-RBT-001) are affected: Part Number 258920028 LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM), Lot QN 200023473; and Part Number 258900029 LABEL, STERILE, IVSTATION SYRINGE (20MMX40MM), Lot QN 200023474. They were recalled due to the potential for a mislabeled syringe produced by the i.v.STATION; 220 units were distributed in Alabama, Maryland and Pennsylvania.
What's being recalled
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.
Recalling firm: Omnicell, Inc., Cranberry Township, PA, United States.
How to identify it
1. Part Number 258920028, Lot Number: QN 200023473. 2. Part Number 258900029, Lot Number: QN 200023474.
The hazard
Potential for mislabeled syringe produced by the i.v.STATION device.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Distribution in Alabama, Maryland and Pennsylvania.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)