Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026

REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve

Ventec Life Systems, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Ventec Life Systems, Inc. · 22002 26th Ave Se · Bothell, WA · 98021-4903

Is this the product you have?

  • REFHF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Lot codes and dates
  • UDI00850018761376/ Serial #s:
    • 25EKMA00BAC
    • 25EKMA009L3
    • 25EKMA009CM
    • 25EKMA009J8
    • 25GKMA00077
    • 25GKMA0007B
    • 25GKMA0009Z
    • 25GKMA0004U
    • 25GKMA000CS
    • 25GKMA000CR
    • 25GKMA000CX
    • 25GKMA000D0
    • 25GKMA000LL
    • 25GKMA000N1
    • 25GKMA000UD
    • 25GKMA000D1
    • 25GKMA000TN
    • 25GKMA000D2
    • 25GKMA000UC
    • 25GKMA000LK
    • 25GKMA000UA
    • 25GKMA000UB
    • 25GKMA000UE
    • 25GKMA000CY
    • 25GKMA000UF
Amount recalled
25 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Labeling; Oxygen Cylinders do not contain required medical gas labeling

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 1:07 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.