Device recall
Z-2415-2023: Snowden-Pencer MIS DIAMOND-TOUCH GRASPER MCKERNAN FUNDUS 5MM, 32CM, RATCHETED…
FDA device recall · Class II · Carefusion 2200 Inc
Key facts
| Recall number (Z-number) | Z-2415-2023 |
|---|---|
| Recall event | 92561 |
| Product | Snowden-Pencer MIS DIAMOND-TOUCH GRASPER MCKERNAN FUNDUS 5MM, 32CM, RATCHETED, REF SP90-7012; endoscopic surgical device |
| Product code | GCJ |
| Recalling firm | Carefusion 2200 Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K930667 |
| FEI number | 3008002452 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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