Device recall
Z-0572-04: Portex Tracheal Tube Guide 15 Fr, non-sterile Catalog Number: 153013
FDA device recall · Class III · Smiths Medical ASD, Inc
Key facts
| Recall number (Z-number) | Z-0572-04 |
|---|---|
| Recall event | 28183 |
| Product | Portex Tracheal Tube Guide 15 Fr, non-sterile Catalog Number: 153013 |
| Product code | BSR |
| Recalling firm | Smiths Medical ASD, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 8, 2012 |
| 510(k) numbers | K902180 |
At a glance
- 1–9 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