Z-2265-2020 Class II Terminated
Recall Details
- Product Type
- Devices
- Report Date
- June 17, 2020
- Initiation Date
- April 20, 2020
- Termination Date
- August 21, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 40 Kits.
Product Description
Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.
Reason for Recall
Custom procedure kits contains affected lots of PosiFlush Syringe, a product recalled by BD.
Distribution Pattern
US nationwide distribution in the states of MO, AR and OK.
Code Information
Lot no. 68336DRW. Item number: 830034. UDI: (01) 10326053106634 (17) 210131 (10) 68336DRW.