Device recall
Z-1127-04: Disposable Oxygen Mask & Bag, Adult Non-Rebreathing Mask w/Safety Vent and 84''…
FDA device recall · Class II · Medex Inc
Key facts
| Recall number (Z-number) | Z-1127-04 |
|---|---|
| Recall event | 29496 |
| Product | Disposable Oxygen Mask & Bag, Adult Non-Rebreathing Mask w/Safety Vent and 84'' Tube; reorder no. 7022; SIngle Patient Only; IPI label - Manufactured by IPI Medical Products, 3217 N. Kilpatrick St., Chicago, IL 60641and Medex label - Manufactured by Medex, Carlsbad, CA 92008 |
| Product code | KGB |
| 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
- 1–9 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