Device recall
Z-2408-2024: Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number…
FDA device recall · Class II · Canadian Hospital Specialties Ltd.
Key facts
| Recall number (Z-number) | Z-2408-2024 |
|---|---|
| Recall event | 94834 |
| Product | Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number: 20400161S Product Description: Laparoscopic Insufflator |
| Product code | GCJ |
| Recalling firm | Canadian Hospital Specialties Ltd. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K001068 |
| FEI number | 3932 |
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