Device recall
Z-1445-2020: Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qty 1, Rx Only…
FDA device recall · Class II · Stryker Corporation
Key facts
| Recall number (Z-number) | Z-1445-2020 |
|---|---|
| Recall event | 84715 |
| Product | Stryker Connected OR Cart,120 V Ref Cat. #240-099-155, Qty 1, Rx Only, Manufactured for: Stryker, 5900 Optical Court, San Jose, CA 95138, UDI: 07613327462784 - Product Usage: The Connect OR Cart is a mobile, medical-grade cart intended to store and transport components of minimally invasive and… |
| Product code | BZN |
| Recalling firm | Stryker Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 3, 2021 |
| FEI number | 2936485 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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