Z-2265-2020 Class II Terminated

Recalled by ROi CPS LLC — Republic, MO

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.