medical MODERATE Updated 2026-04-08

Medline Industries, LP recalls ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

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Recalled Product

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI 10888277314719 (ea) 40888277314710(case) All Lots

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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