What is being recalled?

Medline ENFIT G-Tube Connector Kits containing two SKUs are being recalled due to nonconforming connector dimensions that may not seal properly.

What are the hazards?

Connectors may leak, potentially delaying care and causing fluid loss. Over-tightening can increase infection risk and discomfort.

Are there injuries reported?

No injuries or incidents have been reported to date.

Who should stop using the product?

Patients and healthcare providers who have the recalled kits should stop using them immediately.

What should I do if I own the kit?

Follow the recall notice: stop use, review the SKUs, and contact Medline or your healthcare provider for instructions.

How do I know if my kit is affected?

Check the two SKUs or the UDI-DI codes listed for DYKM2720 and ENFITDISCKIT.

Will I get a refund or replacement?

Medline will provide recall instructions and a remedy. Contact Medline for specifics.

Where can I get more information?

Refer to the FDA recall page linked in the official recall notice.

ENFit is a connector standard for enteral feeding devices intended to prevent misconnections.

What about continuing care while awaiting replacement?

Consult your healthcare provider for interim guidance to minimize risk.

How long might resolution take?

Timelines for refunds or replacements are not specified in the notice.

HIGHFebruary 13, 2026

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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About This Product

Medline ENFIT G-Tube Connector Kits are used in enteral feeding to connect ENFit-style devices. They are provided as part of kits for patient care.

Why This Is Dangerous

Dimensional nonconformity can prevent a proper seal, causing leakage and potential delays in care. Over-tightening can increase infection risk and patient discomfort.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

Leaks could disrupt feeding and care, potentially increasing medical interventions and recovery time.

Practical Guidance

How to identify if yours is affected

Identify if you own DYKM2720 or ENFITDISCKIT kits.
Inspect UDI-DI codes listed for these SKUs.
Stop using affected kits immediately.

Where to find product info

Look for UDI-DI numbers in product labeling or packaging: UDI-DI 10198459016257/40198459016258 and UDI-DI 10193489860078/40193489860079 for ALL LOTS.

What timeline to expect

The recall notice does not specify a refund/replacement timeline. Processing times for medical device recalls vary by program.

If the manufacturer is unresponsive

Contact Medline for instructions.
File a complaint with the FDA if you cannot obtain a remedy from the manufacturer.

How to prevent similar issues

Verify dimensional compatibility of ENFit connectors before use.
Inspect packaging and labeling for ENFit compliance.
Follow up with healthcare providers on device standards and recalls.

Documentation advice

Keep recall notice, document kit lot numbers and UDI-DI codes, save correspondence with Medline, and record dates of action taken.

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.

Reported Incidents

No injuries or incidents have been reported.

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

View Original Recall on FDA - Medical Devices

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Safety Guide

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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

CategoryHealth & Personal Care › Medical Devices

Product TypeENFIT G-Tube Connector Kit

Product Details

Jul 25, 2025

Medline

Medline Industries,