medical MODERATE Updated 2026-09-30

Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D w

See all recalls from Ventec Life Systems, Inc. →

Recalled Product

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

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Hazard / Issue

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI:00850018761376/ 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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for REF: HF2POSTD HomeFill →

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View official government recall

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