Device recall
Z-1269-2025: CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number: SK200FPE…
FDA device recall · Class II · Kung Shin Plastics Co. Ltd.
Key facts
| Recall number (Z-number) | Z-1269-2025 |
|---|---|
| Recall event | 96224 |
| Product | CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number: SK200FPE / 7056) |
| Product code | CAH |
| Recalling firm | Kung Shin Plastics Co. Ltd. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K032878 |
| FEI number | 3004116032 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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