← All recalls
Medical Device

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

Recall date: 2026-04-08 · Source: FDA_DEVICE
Brand / Firm
Medline Industries, LP
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
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.
Units affected
651,789
Description
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
View official recall notice →