HomeFill Oxygen Cylinders
Oxygen cylinders lack required medical gas labeling.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Ventec Life Systems, Inc., of Bothell, Washington, recalled three models of its HomeFill Oxygen System cylinders because they do not contain required medical gas labeling, as stated by the FDA.
The affected products are the HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve, the REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve, and the REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver.
The recall began July 28, 2026, and was added to the FDA's Enforcement Report on September 18, 2026. The products were distributed in Florida, Iowa, Nebraska, Ohio and Tennessee.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
3 products
Affected if its UDI-DI is listed.
REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
- UDI-DI
- 00850018761376
REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver
- UDI-DI
- 00850018761352
HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
- UDI-DI
- 00850018761369
Details
- Company began the recall
- Event ID
- 99660
- Recall numbers
- Z-3221-2026 to Z-3223-2026
- Company
- Ventec Life Systems, Inc.Bothell, Washington
- Hazard
- Labeling error
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
