PlainRecalls
FDA Devices Moderate Class II Terminated

CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) 210930(10)0001304986

Reported: May 6, 2020 Initiated: March 26, 2020 #Z-1795-2020

Product Description

CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) 210930(10)0001304986

Reason for Recall

The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.

Details

Units Affected
900
Distribution
Domestic distribution to the following states: Alabama, Colorado, Illinois, Massachusetts, Missouri, Oklahoma, Rhode Island, Virginia, and Wisconsin.
Location
Franklin Lakes, NJ

Frequently Asked Questions

What product was recalled?
CareFusion Safe-T-Centesis Catheter Drainage Tray, Sterile, For Single Use Only, Rx only, Catalog Number PIG1280T, UDI Number 01)10885403108402(17) 210930(10)0001304986. Recalled by Becton Dickinson & Company. Units affected: 900.
Why was this product recalled?
The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 6, 2020. Severity: Moderate. Recall number: Z-1795-2020.