Device recall
Z-1041-2019: Kendall SCD Express Sterile Sleeves (Thigh Length), Model Number 9736
FDA device recall · Class II · COVIDIEN LLC
Key facts
| Recall number (Z-number) | Z-1041-2019 |
|---|---|
| Recall event | 82245 |
| Product | Kendall SCD Express Sterile Sleeves (Thigh Length), Model Number 9736 |
| Product code | JOW |
| Recalling firm | COVIDIEN LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 24, 2020 |
| 510(k) numbers | K781357 |
| FEI number | 1282497 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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