Avanos CORFLO PEG Kit Recall: Connector May Not Pass Over Guidewire

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Recalling firmAvanos Medical, Inc.5405 Windward Pkwy, N/A · Alpharetta, GA 30004-3894

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Avanos Medical is recalling 2 units per case of CORFLO PEG kits because the connector piece might not pass over the guidewire during medical procedures. This could lead to improper tube placement and potential complications for patients needing long-term feeding.

Why it’s dangerous

The connector piece may not pass over the guidewire during insertion, which could cause the tube to not be properly placed in the stomach. This might lead to complications like tube displacement or improper feeding.

Who’s affected

Patients using the CORFLO PEG kit for medical feeding tubes are affected. Healthcare providers who have the specific catalog numbers and lot numbers listed are most at risk.

How to tell if you have this one

Check for catalog numbers 30-4020 or 30-4320 with specific lot numbers listed in the recall notice. The kits are labeled as CORFLO PEG kits.

Brand
Avanos Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the catalog number and lot numbers to confirm if your kit is affected.

✎ GovInfoNow

Questions people ask

How many units are recalled?

2 units per case.

What is the specific problem with the connector?

The connector piece may not pass over the guidewire during insertion.

What should I do if I have the recalled kit?

The recall notice does not specify a remedy or action steps.

Take action

Contact Avanos Medical

We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0370-2020 — Avanos Medical Avanos Medical

Hello,

I own a Avanos Medical that is covered by recall Z-0370-2020 from Avanos Medical.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0370-2020 (October 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0370-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

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