Device recall
Z-2081-2026: Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
FDA device recall · Class II · BioFire Diagnostics, LLC
Key facts
| Recall number (Z-number) | Z-2081-2026 |
|---|---|
| Recall event | 98719 |
| Product | Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485 |
| Product code | QOF |
| Recalling firm | BioFire Diagnostics, LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K232954 |
| FEI number | 3002773840 |
At a glance
- 1–9 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