Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter
Reported: September 27, 2023 Initiated: August 10, 2023 #Z-2591-2023
Product Description
Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter
Reason for Recall
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Details
- Recalling Firm
- ARROW INTERNATIONAL Inc.
- Units Affected
- 177 units
- Distribution
- US Nationwide distribution.
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter. Recalled by ARROW INTERNATIONAL Inc.. Units affected: 177 units.
Why was this product recalled? ▼
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 27, 2023. Severity: Moderate. Recall number: Z-2591-2023.
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