Medline Industries, LP recalls ENFIT G-TUBE CONNECTOR
- Recalling company
- Medline Industries, LP
- Product
- ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 13, 2026
- Reported
- Apr 8, 2026
- Distribution
- Worldwide - US Nationwide and the countries of Canada.
- Status
- Ongoing
- Quantity
- 651,789
- Lot / codes
- UDI-DI 10888277314719 (ea) 40888277314710(case) All Lots
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1690-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1690-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.