Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Reported: October 11, 2023 Initiated: August 10, 2023 #Z-0002-2024
Product Description
Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
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
- 180 units
- Distribution
- US
- Location
- Morrisville, NC
Frequently Asked Questions
What product was recalled? ▼
Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days. Recalled by ARROW INTERNATIONAL Inc.. Units affected: 180 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 October 11, 2023. Severity: Critical. Recall number: Z-0002-2024.
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