FDA Enforcement
Class II
Terminated
AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018
Recall: Z-0655-2018
·
Reported February 28, 2018
Enforcement
- Recall Number
- Z-0655-2018
- Event ID
- 79197
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Arrow International Inc
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- February 28, 2018
- Initiation Date
- October 17, 2017
- Classification Date
- February 20, 2018
- Termination Date
- April 14, 2020
- Address
- 2400 Bernville Rd, N/A, Reading, PA, 19605-9607, United States
Description
AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018
Reason
These finished good kits may contain the incorrect Springwire Guide (SWG).
Code Info
Lot numbers: Product Codes CDC-42703-XP1A: 23F16M0507 Product Code CDC-47702-XP1A: 23F17A0533
Distribution
Distribution US Nationwide
Quantity
5,926 total