Device recall
Z-1122-04: IPI Ventilator Circuit with 2 Water Traps, product reorder no. 6066; SIngle…
FDA device recall · Class II · Medex Inc
Key facts
| Recall number (Z-number) | Z-1122-04 |
|---|---|
| Recall event | 29496 |
| Product | IPI Ventilator Circuit with 2 Water Traps, product reorder no. 6066; SIngle Patient Use Only; Manufactured by IPI Medical Products, 3217 N. Kilpatrick St., Chicago, IL 60641 |
| Product code | BZO |
| Recalling firm | Medex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2005 |
| FEI number | 1526863 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database