Device recall
Z-1761-2022: NanoSight LM10 fitted with LM12 module. A laboratory instrument for…
FDA device recall · Class II · MALVERN PANALYTICAL LTD
Key facts
| Recall number (Z-number) | Z-1761-2022 |
|---|---|
| Recall event | 90835 |
| Product | NanoSight LM10 fitted with LM12 module. A laboratory instrument for determination of particle characteristics (e.g. size). |
| Product code | REN |
| Recalling firm | MALVERN PANALYTICAL LTD |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3014373630 |
At a glance
- None 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