Device recall
Z-0098-2018: STORZ High Flow Insufflation Tubing (with filter), Catalog #20400161S/10 (outer…
FDA device recall · Class II · Karl Storz Endoscopy
Key facts
| Recall number (Z-number) | Z-0098-2018 |
|---|---|
| Recall event | 78289 |
| Product | STORZ High Flow Insufflation Tubing (with filter), Catalog #20400161S/10 (outer box label), ENDOFLATOR 26-430520-1 also referenced on outer box), individually packaged in a sterile pouch (Catalog #20400161S), 10 pouches per cardboard box. Some of the pouches inside of cardboard box are incorrectly… |
| Product code | NKC |
| Recalling firm | Karl Storz Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 22, 2018 |
| 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