Device recall
Z-2322-2021: RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff…
FDA device recall · Class II · Teleflex Medical Europe Ltd
Key facts
| Recall number (Z-number) | Z-2322-2021 |
|---|---|
| Recall event | 88353 |
| Product | RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100 |
| Product code | BTR |
| Recalling firm | Teleflex Medical Europe Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 24, 2026 |
| 510(k) numbers | K961837 |
| FEI number | 3007134520 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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