REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Ventec Life Systems, Inc. · Labeling; Oxygen Cylinders do not contain required medical gas labeling
Open FDA's page for this record- Cfres ID
- 222117
- Product res number
- Z-3223-2026
- Event date initiated
- 2026-07-28
- Event date posted
- 2026-09-18
- Recall status
- Open, Classified
- Res event number
- 99660
- Product code
- ECX
- Product description
- REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
- Firm FEI number
- 3013095415
- Recalling firm
- Ventec Life Systems, Inc.
- Address 1
- 22002 26th Ave Se
- City
- Bothell
- State
- WA
- Postal code
- 98021-4903
- Additional info contact
- George Koos 1-863-2266285
- Reason for recall
- Labeling; Oxygen Cylinders do not contain required medical gas labeling
- Root cause description
- Process control
- Product quantity
- 25 units
- Distribution pattern
- US Nationwide distribution in the states of FL, IA, OH, NE, TN.
- 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
- 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.
- Harmonized identifiers (openFDA)
- Device name
- Cylinder, Compressed Gas, And Valve
- Medical specialty description
- Anesthesiology
- Regulation number
- 868.2700
- Device class
- 1
- K number
- K053117, K062300, K143060, K142149, K161472, K161179, K771246, K132778, K033897, K153518, K131386, K063354, K101792
- Registration number
- 3008281139, 3013530901, 3005621729, 3034694958, 3008115001, 3023339109, 1937613, 3014810929, 2183615, 3003764448, 3020188747, 9613416, 3005380088, 3012311599, 3013846070, 3012002722, 3008791328
- FEI number
- 3008281139, 3013530901, 3005621729, 3034694958, 3001655525, 3008115001, 3023339109, 1937613, 3014810929, 2183615, 3003764448, 3020188747, 3005380088, 3012311599, 3013846070, 3012002722, 3008791328
