Ventec HomeFill Oxygen System Recalled for Missing Medical Gas Labeling
Ventec Life Systems is recalling two 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 without reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Ventec Life Systems, Inc. is recalling two units of the REF:HF2PC9 HomeFill Oxygen System, specifically the HomeFill Cylinder M9 with Integrated Conserver. The recall is due to a labeling defect where the oxygen cylinders do not contain the required medical gas labeling.
The affected units are identified by UDI 00850018761352 and serial numbers 24IKMA0029J and 24IKMA002CM. These products were distributed nationwide in the states of Florida, Iowa, Ohio, Nebraska, and Tennessee.
Consumers who possess these specific serial numbers should contact Ventec Life Systems for instructions on how to proceed. The recall is classified as Class II by the FDA.
The recalled product
- Product
- REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver
- Manufacturer
- Ventec Life Systems, Inc.
- Hazard
- Affected units
- 2
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UDI:00850018761352/Serial #s: 24IKMA0029J and 24IKMA002CM
Distribution
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