Medline ENFit G-Tube Connector (April 2026)
In plain language
This recall involves Medline ENFit G-Tube Connectors sold in Canada. They are being recalled because they may not form a proper seal, which can lead to leakage. This leakage could delay patient care, especially during medication delivery. Stop using the product and destroy it as instructed in the official notice.
What to do
- Stop using the product immediately.
- Check the model number ENFIT1010GC.
- Destroy the product.
- Contact the manufacturer if you need more information.
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Affected products
ENFit G-Tube Connector
Model: ENFIT1010GC
Lot: All lots
Why this matters
Leakage risk
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: ENFIT1010GC
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Leakage risk
What should consumers do?
Stop using the product immediately. Check the model number ENFIT1010GC. Destroy the product. Contact the manufacturer if you need more information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Leakage risk
When was this product recalled?
This product was recalled on April 8, 2026.
Is the Medline brand affected by this recall?
Yes, Medline products are affected by this recall. This recall involves Medline ENFit G-Tube Connectors sold in Canada. They are being recalled because they may not form a proper seal, which can lead to leakage. This leakage could delay patient care, especially during medication delivery. Stop using the product and destroy it as instructed in the official notice.