FDAFDA · Food and drugs·Recall number Z-0656-2018
ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov 2018
Published February 28, 2018 · Recall initiated: October 17, 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
These finished good kits may contain the incorrect Springwire Guide (SWG).
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Arrow International Inc
- Distributor
- Distribution US Nationwide
- Lot
- Lot numbers: 13F17C0102 and 13F16M0264
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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