HIGH

Medline ENFIT G-Tube Connector Kits Recalled for Leakage Risk in 2026

Medline recalled 9,040 ENFIT G-Tube Connector kits sold worldwide, including the US and Canada. The connectors were not manufactured to required dimensional specifications and may not seal properly with ENFit devices, potentially causing leakage. Stop using the kits immediately and follow recall instructions from Medline or your healthcare provider.

Quick Facts at a Glance

Recall Date
February 13, 2026
Hazard Level
HIGH
Brand
Medline
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter

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Product Details

Kits contained in two SKUs: DYKM2720 G/J TUBE CARE KIT and ENFITDISCKIT ENFIT DISCHARGE KIT. Two UDIs cited for the two SKUs. Distribution: Worldwide, US nationwide and Canada. Quantity: 9,040 kits. All LOTS affected.

The Hazard

Connectors do not meet required dimensional specifications. They may not form a proper seal with ENFit-style devices. Leakage could delay care and result in fluid loss. Over-tightening to stop leakage may increase risk of infection, patient discomfort, and prolonged recovery.

Reported Incidents

No injuries or incidents have been reported.

What to Do

1. Stop using the product immediately. 2. Check if your kit includes SKU DYKM2720 or SKU ENFITDISCKIT. 3. Follow recall instructions and contact Medline Industries, LP or your healthcare provider for guidance. 4. If you require refunds or replacements, follow the recall instructions and contact Medline using the information in the recall notice.

Contact Information

Notification method: Letter. Manufacturer contact as listed in recall materials: Medline Industries, LP. (No phone or website details provided in this summary.)

Key Facts

  • 9,040 total kits recalled
  • Two SKUs affected: DYKM2720 and ENFITDISCKIT
  • US nationwide and Canada distribution
  • UDI-DI identifiers listed for both SKUs
  • High-hazard recall with potential leakage consequences

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Brand
Model Numbers
UDI-DI 10198459016257 (ea) 40198459016258 (case)
UDI-DI 10193489860078 (ea) 40193489860079 (case)
ALL LOTS
Affected States
ALL
Report Date
April 8, 2026
Recall Status
ACTIVE

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