Device recall
Z-1928-2021: Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent
FDA device recall · Class I · Quidel Corporation
Key facts
| Recall number (Z-number) | Z-1928-2021 |
|---|---|
| Recall event | 87996 |
| Product | Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent |
| Product code | QJR |
| Recalling firm | Quidel Corporation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 8, 2022 |
| FEI number | 1000122536 |
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