Device recall
Z-0080-2023: Clip COVID Rapid Antigen Test Kit (25-pack), Catalog Number: MDL002
FDA device recall · Class II · LUMINOSTICS, INC dba CLIP HEALTH
Key facts
| Recall number (Z-number) | Z-0080-2023 |
|---|---|
| Recall event | 90852 |
| Product | Clip COVID Rapid Antigen Test Kit (25-pack), Catalog Number: MDL002 |
| Product code | QKP |
| Recalling firm | LUMINOSTICS, INC dba CLIP HEALTH |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3015104453 |
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