Avanos MIC-KEY Gastric-Jejunal Feeding Tube Kit Recall: Missing Risk Information
Recall of Avanos MIC-KEY Gastric-Jejunal Feeding Tube Kits with missing risk information in instructions. Affected models include non-ENFIT and ENFit connectors. No action required per official notice.
Lower-risk recall
The IFU was missing some risk information requested by another country to be contained in the IFU pertaining to potential complications.
Contact the company
What happened, in plain English
Avanos Medical is recalling certain MIC-KEY Gastric-Jejunal Feeding Tube Kits due to missing risk information in the instructions. This is a non-urgent recall with no action required by the manufacturer. Read more at govinfonow.com/recall/54955-avanos-mic-key-gastric-jejunal-feeding-tube-kit-recall-missing.
Source Summary by GovInfoNow · govinfonow.com/recall/54955-avanos-mic-key-gastric-jejunal-feeding-tube-kit-recall-missing · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2422-2024
Cite this page
“Avanos MIC-KEY Gastric-Jejunal Feeding Tube Kit Recall: Missing Risk Information.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54955-avanos-mic-key-gastric-jejunal-feeding-tube-kit-recall-missing. Based on FDA recall #Z-2422-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2422-2024%22&limit=1).
Why it’s dangerous
The recall is for missing risk information in the instructions that was requested by another country. This means users might not have the full safety details needed for proper use, but it does not indicate an immediate physical hazard.
Who’s affected
Patients using these feeding tube kits for medical nutrition support. Healthcare providers who have the affected models may be at risk if they use the kits without updated instructions.
How to tell if you have this one
Check for product codes starting with 0270- or 8270- followed by the size (e.g., 14 Fr, 16 Fr) and the specific UDI-DI numbers listed in the recall notice. All lot numbers are affected.
- Brand
Avanos- Category
Medical device
What to do — step by step
Check Product Details
Review the product code and UDI-DI numbers to confirm if your kit is affected. The recall includes specific models with non-ENFIT and ENFit connectors.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide - There was also government and military distribution and the countries of Canada and Australia.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-2422-2024 (May 31, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2422-2024 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.