BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect
(BMC), Beijing, China, retrospectively reported to the US Food and Drug Administration (FDA) a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect. On August 19, 2026, the FDA classified this retrospective recall as a Class I recall (FDA Recall Number: Z-2979-2026). BMC has identified that firmware version, G3-2.00.76 installed on these Luna G3 APAP (Model LG3600) devices contained a firmware defect.
FDA recall noticesThis row is from FDA’s lot file, which does not include a public page per product. The button opens FDA’s published recall list.
What to do
- 1Do not eat or serve it.
- 2Throw it away or return it to the store.
- 3If you already ate it and feel sick, contact a doctor.
Recall details
- Firm
- BMC Medical Co., Ltd.
- Status
- Announced
- Reported
- Sep 8, 2026
- Started
- Sep 8, 2026
- Where sold
- the United States due to firmware defect
- Notice number
- BMC%20Medical%20Co.,%20Ltd.%20Recalls%20Luna%20G3%20APAP%20(Model%20LG3600)%20with%20Firmware%20G3-2.00.76%20Due%20to%20Firmware%20Defect
Lots, UPC, dates
No lot or UPC details were listed.
Agency wording
BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect
Source: FDA notice. This is not medical advice. Compare your package codes before you act.