ROi CPS LLC: Medical Device Recall in 2020 - (Recall #: Z-2265-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.

Product Classification:

Class II

Date Initiated: April 20, 2020

Date Posted: June 17, 2020

Recall Number: Z-2265-2020

Event ID: 85591

Reason for Recall:

Custom procedure kits contains affected lots of PosiFlush Syringe, a product recalled by BD.

Status: Terminated

Product Quantity: 40 Kits.

Code Information:

Lot no. 68336DRW. Item number: 830034. UDI: (01) 10326053106634 (17) 210131 (10) 68336DRW.

Distribution Pattern:

US nationwide distribution in the states of MO, AR and OK.

Voluntary or Mandated:

Voluntary: Firm initiated