← FDA ENFORCEMENT
Z-3222-2026Class II

Ventec Life Systems, Inc.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Ventec Life Systems, Inc.
Product type
Device
Status
Ongoing
Report date
2026-09-30
Distribution
US Nationwide distribution in the states of FL, IA, OH, NE, TN.
Firm state
WA
Product quantity
2 units
Initiated by
Voluntary: Firm initiated
Reason for recall

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Product description

REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 with Integrated Conserver

Code / lot info

UDI:00850018761352/Serial #s: 24IKMA0029J and 24IKMA002CM

Other recalls SPEQ maps to Documentation & Change Control
See all Documentation & Change Control recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →