REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
FDA Recall Z-3223-2026 · Posted 2026-09-18
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Recalling FirmVentec Life Systems, Inc.
Recall StatusOpen, Classified
Product CodeECX
Date Initiated2026-07-28
Product Quantity25 units
Reason for Recall
Labeling; Oxygen Cylinders do not contain required medical gas labeling
Firm Action
On July 28, 2026, Ventec Life Systems Inc. issued a Urgent: Medical Device Recall notification to affected consignees via: certified mail. Ventec ask consignees to take the following actions:
1. Immediately discontinue use of affected HomeFill Oxygen Cylinders.
2. Inspect current stock, quarantine/segregate any unused affected products, remove affected product from clinical service and segregate to prevent further use until the enclosed label correction has been completed.
3. Use an unaffected oxygen cylinder for patient support.
4. If you have distributed or transferred affected product to other facilities, caregivers, or end users, you must promptly notify them of this recall and provide a copy of this notification.
5.. Confirm receipt of this notification letter by returning the enclosed Customer Response Form to React Health WITHIN 7 DAYS OF RECEIPT.
6. Upon receipt of the Customer Response Form, React Health will arrange for shipment of the label and instructions to apply the label to affected cylinders along with an update confirmation letter.
7. Update the affected product and return the completed confirmation letter to React Health. Contact Customer Support at 863-226 -6285 to discuss completing the form, if necessary.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution in the states of FL, IA, OH, NE, TN.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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