Medline Industries, LP recalls ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

Recall date

February 13, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1690-2026

FDA classification

Class II

Brand / firm

Medline Industries, LP

Sold / distributed

Worldwide - US Nationwide and the countries of Canada.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC