Ventec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
Ventec Life Systems is recalling 25 HomeFill Oxygen Systems because the cylinders 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 required medical gas labeling) without reported injuries or illnesses, fitting the criteria for a moderate severity recall.
Plain-English summary
Ventec Life Systems, Inc. is recalling 25 units of the HomeFill Oxygen System, specifically the HomeFill cylinder D 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 UDI 00850018761376 and specific serial numbers listed in the agency records.
Consumers with these specific serial numbers should stop using the product and contact Ventec Life Systems for instructions on how to proceed.
The recalled product
- Product
- REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
- Manufacturer
- Ventec Life Systems, Inc.
- Hazard
- Affected units
- 25
Distribution
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