Avanos CORFLO Safety PEG Kit Recall
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Updated April 30, 2026
Avanos Medical is recalling CORFLO Safety PEG kits with ENFit connectors because they contain lidocaine injection from a supplier with quality issues. This could affect the safety and sterility of the product.
Is the Avanos Medical, Inc. recalled? Yes. This product was recalled by FDA on April 30, 2026. Details below.
What is recalled
CORFLO Safety PEG Kit with ENFit Connector, Model/Catalog Number 50-5320, made by Avanos Medical, Inc.
Am I affected
You're affected if you have a CORFLO Safety PEG Kit with ENFit Connector, Model 50-5320 from Avanos Medical in your possession or use.
What to do right now
Stop using this product immediately. Contact Avanos Medical or your healthcare provider for instructions on return or replacement.
The hazard
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-2338-2026
- Classification
- Class II
- Recalled
- April 30, 2026
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