Device recall
Z-1956-2019: Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.
FDA device recall · Class I · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-1956-2019 |
|---|---|
| Recall event | 83202 |
| Product | Sheridan Endotracheal Tube contained inside Centurion kit code TC7855. |
| Product code | BTR |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 28, 2020 |
| 510(k) numbers | K091761, K822082 |
| FEI number | 3008403546 |
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