Z-2556-2019 Class II Terminated
FDA device recall Z-2556-2019 was initiated by Arrow International Inc on August 6, 2019 and is designated Class II. Reason for recall: Products may contain the incorrect banner card within the kit The recall status is terminated (terminated September 29, 2020). Affected quantity: 231 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 2, 2019
- Initiation Date
- August 6, 2019
- Termination Date
- September 29, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 231 units
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
Distribution Pattern
US Nationwide distribution.
Code Information
Lot Number: 13F18H0499