Device recall
Z-1010-2026: Kii Low Profile, Bladed Dual Pack, Qty. 1 5x55mm REF: CTB23
FDA device recall · Class II · Applied Medical Resources Corp
Key facts
| Recall number (Z-number) | Z-1010-2026 |
|---|---|
| Recall event | 98191 |
| Product | Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 |
| Product code | GCJ |
| Recalling firm | Applied Medical Resources Corp |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K060096 |
| FEI number | 2027111 |
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