Device recall
Z-0323-2023: Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B
FDA device recall · Class I · DEWEI MEDICAL EQUIPMENT CO LTD
Key facts
| Recall number (Z-number) | Z-0323-2023 |
|---|---|
| Recall event | 91137 |
| Product | Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B |
| Product code | QBD |
| Recalling firm | DEWEI MEDICAL EQUIPMENT CO LTD |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3016853433 |
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