Medical Device Recall: ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Medline Industries, LP · February 13, 2026
Reason for Recall
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.
Distribution
Worldwide - US Nationwide and the countries of Canada.
States Affected
NATIONWIDE
Quantity Affected
651,789
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1690-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.