Device recall
Z-1618-2020: Karl Storz SE & Co. KG, C-MAC Video Laryngoscope MIL # 1, for the following REF…
FDA device recall · Class II · Karl Storz Endoscopy
Key facts
| Recall number (Z-number) | Z-1618-2020 |
|---|---|
| Recall event | 85089 |
| Product | Karl Storz SE & Co. KG, C-MAC Video Laryngoscope MIL # 1, for the following REF numbers: 1. 8403xx series, which includes: 8403AX, AXC, BX, BXC, DXC, EXC, GXC, HX, HXK, HXP, KXC, MXC 2. 8401xx series, which includes: 8401AX, AXC, BX, BXC, DXC, GXC, HX, HXP, KXC. Product Usage: Video Laryngoscopes… |
| Product code | EQN |
| Recalling firm | Karl Storz Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 1, 2022 |
| FEI number | 3007475226 |
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