Recall
FDAHealthFebruary 13, 2026

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

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
February 13, 2026

Worldwide - US Nationwide and the countries of Canada.

What's affected?

Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Lot code
s

Additional details

UDI-DI 10888277314719 (ea) 40888277314710(case) All Lots

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 651,789.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.