FDAFDA · Food and drugs·Recall number Z-3221-2026
HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
Published September 30, 2026 · Recall initiated: July 28, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling; Oxygen Cylinders do not contain required medical gas labeling
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Ventec Life Systems, Inc.
- Distributor
- US Nationwide distribution in the states of FL, IA, OH, NE, TN.
- Lot
- UDI:00850018761369/Serial #s: 24IKMA00532 24IKMA0053M 24IKMA0054N 24IKMA005G8 24IKMA005AP 24IKMA005QB 24IKMA005Q4 24IKMA005PM 24IKMA005QJ 24IKMA005QX 24IKMA005PJ 24IKMA005SW 24IKMA005RB 24IKMA00612 24IKMA0067E 24IKMA0066L 24IKMA0068U 24IKMA00685 24IKMA006AQ 24IKMA006B7 24IKMA006BG
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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Questions about this recall
Was HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recalled?
Yes. FDA published recall Z-3221-2026 on September 30, 2026. Reported hazard: Labeling; Oxygen Cylinders do not contain required medical gas labeling
What should I do if I have this product?
Voluntary: Firm initiated · Letter
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