Device recall
Z-1349-2024: microStar Reader, Model Numbers: 10015-000 (marketed in EMEA as 100, 102, 110…
FDA device recall · Class II · Landauer
Key facts
| Recall number (Z-number) | Z-1349-2024 |
|---|---|
| Recall event | 94043 |
| Product | microStar Reader, Model Numbers: 10015-000 (marketed in EMEA as 100, 102, 110, and 201), 10016-000 (marketed in EMEA as 101), 10036-000, 10044-000, 10055-000, BC30058, and BC30059 |
| Product code | LHO |
| Recalling firm | Landauer |
| Recall class | Class II |
| Status | Completed |
| FEI number | 3008426232 |
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