PlainRecalls
FDA Devices Moderate Class II Terminated

ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLACEMENT

Reported: October 28, 2015 Initiated: May 21, 2015 #Z-0132-2016

Product Description

ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLACEMENT

Reason for Recall

Potential for a leak at the tubing to luer bond.

Details

Recalling Firm
Baxter Healthcare Corp
Units Affected
23,600
Distribution
Domestic Only
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLACEMENT. Recalled by Baxter Healthcare Corp. Units affected: 23,600.
Why was this product recalled?
Potential for a leak at the tubing to luer bond.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 28, 2015. Severity: Moderate. Recall number: Z-0132-2016.