FDADecember 19, 2025device

Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear; may result in fluid leaks, occluded fluid flow, inability to inject/withdraw blood product, delayed/interrupted therapy, exposure to biological contaminants, air infused into the body

What to do

FDA enforcement status: Ongoing

Brands named

icu medicalicu

UPCs

0084061902605900840619006785

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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