Device recall
Z-1284-2024: CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c)…
FDA device recall · Class I · Medos International Sarl
Key facts
| Recall number (Z-number) | Z-1284-2024 |
|---|---|
| Recall event | 93955 |
| Product | CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; Vascular guide-catheter, single-use |
| Product code | QJP |
| Recalling firm | Medos International Sarl |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K192804 |
| FEI number | 3008114965 |
At a glance
- 1–9 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