FDAFDA · Food and drugs·Recall number Z-3223-2026
REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D 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: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 25GKMA000UF
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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Questions about this recall
Was REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve recalled?
Yes. FDA published recall Z-3223-2026 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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