Baxter Healthcare Corporation recalls Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid Displac

Recalled February 17, 2021 · FDA recall Z-1102-2021 · Baxter Healthcare

Hazard

There were customer reports of separation between the tubing and Male Luer Lock Adaptor. · FDA Class II

Units

66,800 units

Sold at

Worldwide distribution - US Nationwide distribution in the states of SC, OH, MI, CA, TX, and the countries of UK, Ireland.

Description

There were customer reports of separation between the tubing and Male Luer Lock Adaptor.

Product

Baxter ONE-LINK Non-DEHP Y-Type Microbore Catheter Extension Set, Bonded Needle-free IV Connector, Neutral Fluid Displacement, 5.7 " (14 cm), REF 7N8370K - Product Usage: intended for single patient use with a vascular access device for the administration of drugs and solutions without needles, thus eliminating the potential for needle-stick injuries during use.

Manufacturer(s)

Baxter Healthcare Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →