Ventec recalls HomeFill oxygen cylinders over missing required medical gas labeling
The HomeFill oxygen cylinders do not carry the medical gas labeling that is required, so users may not have the label information meant to go with the oxygen.
What to do
The notice does not give instructions. Read the official notice for details.
Do not stop taking a prescribed medicine, or stop using a device you rely on, until you have talked to your pharmacist or doctor.
Recall details
- Product
- REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve; REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver; HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
- Company
- Ventec Life Systems, Inc.
- Hazard
- Labeling; Oxygen Cylinders do not contain required medical gas labeling
- Units
- 25 units; 2 units; 21 units
- Where sold
- US Nationwide distribution in the states of FL, IA, OH, NE, TN.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- September 18, 2026
- Recall started
- July 28, 2026
- FDA enforcement report
- September 30, 2026
- Identifiers
- Codes: 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
- FDA recall number: Z-3223-2026
- Codes: UDI:00850018761352/Serial #s: 24IKMA0029J and 24IKMA002CM
- FDA recall number: Z-3222-2026
- Codes: 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
- FDA recall number: Z-3221-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve | REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver | HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
- Reason for recall
- Labeling; Oxygen Cylinders do not contain required medical gas labeling
- Classification
- Class II (Ongoing)
- Distribution
- US Nationwide distribution in the states of FL, IA, OH, NE, TN.
- Quantity
- 25 units; 2 units; 21 units
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