FDAFDA · Food and drugs·Recall number Z-2590-2023
Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular
Published September 27, 2023 · Recall initiated: August 10, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
What to do
Voluntary: Firm initiated
Recall details
- Manufacturer
- ARROW INTERNATIONAL Inc.
- Distributor
- US Nationwide distribution.
- Lot
- Batch/Lot number 13F22J0617
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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