Avanos Medical, Inc. Recall
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Updated April 30, 2026
Avanos Medical, Inc. is recalling Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320. Hazard: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Is the Avanos Medical, Inc. recalled? Yes. This product was recalled by FDA on April 30, 2026. Details below.
What is recalled
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Am I affected
You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.
What to do right now
Voluntary: Firm initiated
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
- Drugs & Medications
- Recall ID
- fda-Z-2338-2026
- Classification
- Class II
- Recalled
- April 30, 2026
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