medical MODERATE Updated 2026-09-30

Ventec Life Systems, Inc. recalls REF:HF2PC9 HomeFill Oxygen System, HomeFill Cylinder M9 wit

See all recalls from Ventec Life Systems, Inc. →

Recalled Product

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

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

Labeling; Oxygen Cylinders do not contain required medical gas labeling

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI:00850018761352/Serial #s: 24IKMA0029J and 24IKMA002CM

✅ 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:HF2PC9 HomeFill Oxygen →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Medline Industries, LP recalls Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DY

2026-09-30 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

Medline Industries, LP recalls Medline Convenience Kits: 1) PEDS SINUS PACK, Catalog Numbe

2026-09-30 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

Philips North America Llc recalls SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T

2026-09-30 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

Philips North America Llc recalls Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initi

2026-09-30 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.