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Medical device recall · FDA · Published July 28, 2026

Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve

Ventec Life Systems recalls HomeFill oxygen cylinders with CGA870 Post Valve that lack required medical gas labeling. Consumers should check serial numbers listed to determine if affected.

🇺🇸 FDA recall #Z-3223-2026Medical deviceVentec Life Systems ›
✎ GovInfoNow plain-language explainer

What happened, in plain English

Ventec Life Systems is recalling HomeFill oxygen cylinders with CGA870 Post Valve that do not have required medical gas labeling. This could lead to incorrect gas usage if the cylinders are not properly labeled. Read more at govinfonow.com/recall/1292724-ventec-homefill-oxygen-cylinder-lacks-required-medical-gas-labeling.

Source Summary by GovInfoNow · govinfonow.com/recall/1292724-ventec-homefill-oxygen-cylinder-lacks-required-medical-gas-labeling · Published October 6, 2026 · Updated October 6, 2026 · FDA enforcement record: FDA #Z-3223-2026

Cite this page

“Ventec HomeFill Oxygen Cylinder Lacks Required Medical Gas Labeling.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1292724-ventec-homefill-oxygen-cylinder-lacks-required-medical-gas-labeling. Based on FDA recall #Z-3223-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3223-2026%22&limit=1).

Why it’s dangerous

Oxygen cylinders must have specific medical gas labeling to ensure they contain the correct type of oxygen for medical use. Without this labeling, users might mistakenly use the wrong gas, which could be dangerous for medical applications.

Who’s affected

Home oxygen users who own the specific HomeFill cylinders with CGA870 Post Valve and serial numbers listed in the recall. Those with medical oxygen needs are most at risk.

How to tell if you have this one

Check if your HomeFill oxygen cylinder has a CGA870 Post Valve and one of the listed serial numbers: 25EKMA00BAC, 25EKMA009L3, 25EKMA009CM, 25EKMA009J8, 25GKMA00077, 25GKMA0007B, 25GKMA0009Z, 25GKMA0004U, 25GKMA000CS, 25GKMA000CR, 25GKMA000CX, 25GKMA000D0, 25GKMA000LL, 25GKMA000N1, 25GKMA000UD, 25GKMA000D1, 25GKMA000TN, 25GKMA000D2, 25GKMA000UC, 25GKMA000LK, 25GKMA000UA, 25GKMA000UB, 25GKMA000UE, 25GKMA000CY, 25GKMA000UF.

  • Brand
    Ventec Life Systems
  • Category
    Medical device
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    US Nationwide distribution in the states of FL, IA, OH, NE, TN.
Recall numberProduct, codes & lotsQuantity
Z-3221-2026HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve; UDI:00850018761369/Serial #s: 24IKMA00532 24IKMA0053M 24IKMA0054N 24IKMA005G8 24IKMA005AP 24IKMA005QB 24IKMA005Q4 24IKMA005PM 24IKMA005QJ 24IKMA005QX 24IKMA005PJ 24IKMA005SW 24IKMA005RB 24IKMA00612 24IKMA0067E 24IKMA0066L 24IKMA0068U 24IKMA00685 24IKMA006AQ 24IKMA006B7 24IKMA006BG21 units
Z-3222-2026REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver; UDI:00850018761352/Serial #s: 24IKMA0029J and 24IKMA002CM2 units
Z-3223-2026REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve; UDI:00850018761376/ Serial #s: 25EKMA00BAC 25EKMA009L3 25EKMA009CM 25EKMA009J8 25GKMA00077 25GKMA0007B 25GKMA0009Z 25GKMA0004U 25GKMA000CS 25GKMA000CR 25GKMA000CX 25GKMA000D0 25GKMA000LL 25GKMA000N1 25GKMA000UD 25GKMA000D1 25GKMA000TN 25GKMA000D2 25GKMA000UC 25GKMA000LK 25GKMA000UA 25GKMA000UB 25GKMA000UE 25GKMA000CY 25GKMA000UF25 units
Based on the official FDA remedy

What to do — step by step

  1. Check Cylinder Labeling

    Look for required medical gas labeling on the cylinder. If missing, it is part of the recall.

✎ GovInfoNow

Questions people ask

Do I need to stop using this oxygen cylinder?

No, but you should check if it has the required medical gas labeling. If missing, it is part of the recall.

What should I do if my cylinder has the correct labeling?

No action is needed if your cylinder has the required medical gas labeling.

How can I find out if my cylinder is affected?

Check the serial number against the list provided in the recall notice.

Take action

Contact Ventec Life Systems

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

Subject: Recall Z-3223-2026 — Ventec Life Systems Ventec Life Systems

Hello,

I own a Ventec Life Systems that is covered by recall Z-3223-2026 from Ventec Life Systems.

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-3223-2026 (July 28, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3223-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA