Medline recalls two kits with ENFIT G-Tube connectors that may leak due to improper sealing, risking fluid loss and infection. Affected kits have specific SKUs and UDI codes.
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.
Medline is recalling two kits that include ENFIT G-Tube connectors. These connectors may not seal properly, leading to leaks that could cause fluid loss, infection, or delayed care. Using them without fixing the issue could harm patients.
The connectors were made to incorrect sizes and may not seal tightly with ENFit devices. This can cause leaks, which might lead to fluid loss or infection if the user tries to fix it by over-tightening.
Patients using home care for tube feeding or drainage systems who own the recalled Medline kits are most at risk. Healthcare providers using these kits for patient care may also be affected.
Check for the SKUs DYKM2720 (G/J Tube Care Kit) or ENFITDISCKIT (ENFIT Discharge Kit). The kits have specific UDI codes: 10198459016257 (single unit) or 10193489860078 (single unit).
Look for the SKUs DYKM2720 or ENFITDISCKIT on the kit packaging.
Reach out to Medline directly for assistance with the recall.
The connectors were not made to the correct size and may not seal properly with ENFit devices, which could cause leaks and lead to fluid loss or infection.
Check for the SKUs DYKM2720 (G/J Tube Care Kit) or ENFITDISCKIT (ENFIT Discharge Kit) with UDI codes 10198459016257 or 10193489860078.
Contact Medline directly for assistance with the recall. They may provide a remedy or guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1691-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1691-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
