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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Medline
- Product type
- ENFIT G-Tube Connector Kit
- Model numbers
- UDI-DI 10198459016257 (ea) 40198459016258 (case), UDI-DI 10193489860078 (ea) 40193489860079 (case), ALL LOTS
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
February 13, 2026
Reported by FDA DEVICE
April 8, 2026
RecallRadar source check
April 15, 2026
Consumer action
Use the official remedy and keep documentation.
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
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.
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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.
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
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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