FDAFDA · Food and drugs·Recall number Z-0076-2015
Multi-Lumen Central Venous Catheterization Kit
Published October 22, 2014 · Recall initiated: September 18, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Arrow International Inc
- Distributor
- US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.
- Lot
- Catolog No - AK-12703 lot number RF3039028
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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