Device recall
Z-0073-2019: smiths medical portex First Breath Adult Nasal Cannula, REF 001289, Curved…
FDA device recall · Class III · Smiths Medical ASD Inc.
Key facts
| Recall number (Z-number) | Z-0073-2019 |
|---|---|
| Recall event | 80635 |
| Product | smiths medical portex First Breath Adult Nasal Cannula, REF 001289, Curved Flared Tips, 213 cm (7 ft.) Tubing, Over-the-Ear Style. Product Usage: For the administration of nasal oxygen and humidity to patients. |
| Product code | CAT |
| Recalling firm | Smiths Medical ASD Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 30, 2019 |
| FEI number | 3012307300 |
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