FDAFebruary 13, 2026device

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

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

The hazard

Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lpmedlinemedline industries

UPCs

1088827731471940888277314710

Recall history

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

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ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC — Recall Details · AllClear