CanadaMedline ENFit G‑Tube Connector (model ENFIT1010GC, all lots) is affected; look for the ENFit G‑Tube Connector labeled ENFIT1010GC. It was recalled because it was not manufactured to required dimensional specifications and may not form a proper seal with ENFit devices, risking leakage that can delay patient care during medication delivery. Customers should destroy this product and contact the manufacturer if they require additional information.
What's being recalled
Companies: Medline Industries, LP, Three Lakes Drive, Northfield, Illinois, United States, 60093.
How to identify it
Affected products: ENFit G-Tube Connector; Lot or serial number: All lots.; Model or catalogue number: ENFIT1010GC
The hazard
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
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States