Device recall
Z-1978-2021: NeuMoDx Cartridge, For In Vitro Diagnostic Use on the NeuMoDx 288 and NeuMoDx 96…
FDA device recall · Class II · NeuMoDx Molecular Inc
Key facts
| Recall number (Z-number) | Z-1978-2021 |
|---|---|
| Recall event | 88099 |
| Product | NeuMoDx Cartridge, For In Vitro Diagnostic Use on the NeuMoDx 288 and NeuMoDx 96 Molecular Systems, Model Number 100100 |
| Product code | QJR |
| Recalling firm | NeuMoDx Molecular Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2022 |
| FEI number | 3010729479 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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