Ventec HomeFill Oxygen Cylinder Recall for Missing Medical Gas Labeling
Ventec Life Systems is recalling 21 HomeFill Oxygen System cylinders because they lack required medical gas labeling.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error (missing medical gas labeling) without reported injuries or illnesses, which aligns with the 'Moderate' severity criteria for minor labeling errors.
Plain-English summary
Ventec Life Systems, Inc. is recalling 21 units of the HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve. The recall was initiated because the oxygen cylinders do not contain the required medical gas labeling.
The affected units were distributed nationwide in the states of Florida, Iowa, Ohio, Nebraska, and Tennessee. The recall is identified by FDA recall number Z-3221-2026.
Consumers who have these specific cylinders should contact Ventec Life Systems, Inc. for instructions on how to proceed with the recall.
The recalled product
- Product
- HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve
- Manufacturer
- Ventec Life Systems, Inc.
- Hazard
- Affected units
- 21
Distribution
Related recalls
Same manufacturer · Ventec Life Systems, Inc.
See all →- ModerateVentec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
FDA (Devices) · 2026-09-30
- ModerateVentec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
FDA (Devices) · 2026-09-30
- SevereVOCSN+Pro Respiratory System Backup Battery Alarm Failure Recall
FDA (Devices) · 2026-07-01
- SevereVOCSN V+Pro Ventilator System Respiratory Device Safety Recall
FDA (Devices) · 2026-05-13
- SevereVentec VOCSN Ventilators Recalled Due to Incorrect Service Parts
FDA (Devices) · 2025-03-05
Same hazard · mis labeling
See all →- ModerateBaxter PRO+ Mattress Recalled for UDI Labeling Error
FDA (Devices) · 2026-09-30
- HighWhole Foods Market Recalls Cabricharme Cheese for Undeclared Egg Allergen
FDA (Food) · 2026-09-30
- ModerateOlympus Endoscopic Balloon Dilator Recalled for Incorrect Inflation Chart Label
FDA (Devices) · 2026-09-30
- ModerateBaxter Recalls PRO+ MRS Mattress Due to UDI Labeling Error
FDA (Devices) · 2026-09-30
- HighBecton, Dickinson ForeSight Elite Tissue Oximetry Cable Recall for Incorrect Channel Switching
FDA (Devices) · 2026-09-30