Device recall
Z-2930-2026: GLIDESHEATH SLENDER A-KIT 6F 10CM.021GW. 5 units per box. Product Code…
FDA device recall · Class II · Terumo Medical Corporation
Key facts
| Recall number (Z-number) | Z-2930-2026 |
|---|---|
| Recall event | 99285 |
| Product | GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery. |
| Product code | DYB |
| Recalling firm | Terumo Medical Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K173831 |
| FEI number | 1118880 |
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