Z-3223-2026 Class II Ongoing
FDA device recall Z-3223-2026 was initiated by Ventec Life Systems, Inc. on Jul 28, 2026 and is designated Class II. Reason for recall: Labeling; Oxygen Cylinders do not contain required medical gas labeling The recall status is ongoing. Affected quantity: 25 units.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 30, 2026
- Initiation Date
- Jul 28, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 25 units
Product Description
REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Reason for Recall
Labeling; Oxygen Cylinders do not contain required medical gas labeling
Distribution Pattern
US Nationwide distribution in the states of FL, IA, OH, NE, TN.
Code Information
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