FDAFDA · Food and drugs·Recall number Z-2327-2017
Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Published June 21, 2017 · Recall initiated: May 9, 2017
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 is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Arrow International Inc
- Distributor
- Worldwide Distribution - US (nationwide) and Canada
- Lot
- Material number: ASK-04018-CC, ASK-04510-HUM, ASK-04550-UHC, Device Listing D025180
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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