Drug recall
BMC/REACTHEALTH Luna G3 APAP REF LG 3600
FDA recall event 99445 · Class I · BMC Medical Co., Ltd.
Key facts
| Event ID | 99445 |
|---|---|
| Recall numbers | Z-2979-2026 |
| Recalling firm | BMC Medical Co., Ltd. |
| Product type | Devices |
| Products | BMC/REACTHEALTH Luna G3 APAP REF LG 3600 |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse |
| Initiation date | Jul 15, 2026 |
| Report date | Aug 26, 2026 |
| City | Beijing |
| Country | China |
| FEI number | 3008566132 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: