Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
Reported: October 2, 2019 Initiated: August 6, 2019 #Z-2556-2019
Product Description
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
Reason for Recall
Products may contain the incorrect banner card within the kit
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- 231 units
- Distribution
- US Nationwide distribution.
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.. Recalled by Arrow International Inc. Units affected: 231 units.
Why was this product recalled? ▼
Products may contain the incorrect banner card within the kit
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 2, 2019. Severity: Moderate. Recall number: Z-2556-2019.
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