- Recalling firm
- Ventec Life Systems, Inc.
- Reason for recall
- Labeling; Oxygen Cylinders do not contain required medical gas labeling
- Affected products (lot / model / serial)
- 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
- Units affected
- 25 units
- Distribution pattern
- US Nationwide distribution in the states of FL, IA, OH, NE, TN.
- Firm location
- Bothell, WA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3223-2026
- Recall initiated
- July 28, 2026
- FDA classification date
- September 18, 2026
- FDA report date
- September 30, 2026
- FDA event ID
- 99660
- Last updated on HTM Vibe
- October 6, 2026
