Device recall
Z-1957-2023: Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff…
FDA device recall · Class I · TELEFLEX LLC
Key facts
| Recall number (Z-number) | Z-1957-2023 |
|---|---|
| Recall event | 92373 |
| Product | Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080 |
| Product code | BTR |
| Recalling firm | TELEFLEX LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K931164 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 100–999 Products in the same recall event
- 100–999 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