Device recall
Z-1398-2022: HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59…
FDA device recall · Class I · Haimen Shengbang Laboratory Equipment Co. Ltd.
Key facts
| Recall number (Z-number) | Z-1398-2022 |
|---|---|
| Recall event | 90602 |
| Product | HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59 Activated Type |
| Product code | QMC |
| Recalling firm | Haimen Shengbang Laboratory Equipment Co. Ltd. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3011676045 |
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