Device recall
Z-2979-2026: BMC/REACTHEALTH Luna G3 APAP REF LG 3600
FDA device recall · Class I · BMC Medical Co., Ltd.
Key facts
| Recall number (Z-number) | Z-2979-2026 |
|---|---|
| Recall event | 99445 |
| Product | BMC/REACTHEALTH Luna G3 APAP REF LG 3600 |
| Product code | MNS |
| Recalling firm | BMC Medical Co., Ltd. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 3008566132 |
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