Official recall record
Medline ENFit G-Tube Connector
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-04-09
- Last updated (per notice)
- 2026-04-08
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Medline ENFit G-Tube Connector (ENFIT1010GC) is recalled. This connector was not manufactured to the required dimensional specifications. Thus, the connector may not form a proper seal with ENFit style devices, so lead to leakage. This may delay the patient care, particularly during medication delivery. Customers should destroy this product.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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