Device recall
Z-1381-2019: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part…
FDA device recall · Class II · Dornier Medtech America, Inc.
Key facts
| Recall number (Z-number) | Z-1381-2019 |
|---|---|
| Recall event | 82625 |
| Product | Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers Part Number/Description: K1001291 600 micron single use fiber K2011824 600 micron single use fiber K1001293 600 micron single use fiber K2011826 600 micron 5X reusable fiber K1008084 600 micron single use fiber K2011828 400 micron… |
| Product code | GEX |
| Recalling firm | Dornier Medtech America, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2020 |
| 510(k) numbers | K083500 |
| FEI number | 1037955 |
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