Device recall
Z-2541-2014: H4052 Endo Tube Holder, Pedi 3.0mm Pediatric Endotracheal Intubation Kit
FDA device recall · Class I · Smiths Medical ASD, Inc.
Key facts
| Recall number (Z-number) | Z-2541-2014 |
|---|---|
| Recall event | 68739 |
| Product | H4052 Endo Tube Holder, Pedi 3.0mm Pediatric Endotracheal Intubation Kit |
| Product code | BTR |
| Recalling firm | Smiths Medical ASD, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 26, 2021 |
| FEI number | 1217052 |
At a glance
- None 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