Device recall
Z-1908-2025: Sample probe sucks a sample dispensed into a tube or cup and discharges the…
FDA device recall · Class II · Beckman Coulter Mishima K.K.
Key facts
| Recall number (Z-number) | Z-1908-2025 |
|---|---|
| Recall event | 96748 |
| Product | Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670 |
| Product code | JJE |
| Recalling firm | Beckman Coulter Mishima K.K. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K961274 |
| FEI number | 3002807663 |
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