PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: June 17, 2020 Initiated: April 20, 2020 #Z-2265-2020

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.

Details

Recalling Firm
ROi CPS LLC
Units Affected
40 Kits.
Distribution
US nationwide distribution in the states of MO, AR and OK.
Location
Republic, MO

Frequently Asked Questions

What product was recalled?
Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy.. Recalled by ROi CPS LLC. Units affected: 40 Kits..
Why was this product recalled?
Custom procedure kits contains affected lots of PosiFlush Syringe, a product recalled by BD.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 17, 2020. Severity: Moderate. Recall number: Z-2265-2020.