BMC Medical Co., Ltd. Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect recalled over See official notice
What to do
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Confirm the details against the official FDA notice before acting.
Does this affect you?
Check the product in your home against the recalled item:
Full recall details
- Reason for recall
- On July 15, 2026, BMC Medical Co., Ltd. (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. This corrective action was not reported to customers. O
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- BMC Medical Co., Ltd.
- Recall type
- Voluntary
- Quantity
- Distribution
Frequently asked questions
Is BMC Medical Co., Ltd. Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect recalled?
Yes. It was recalled on September 7, 2026 because on July 15, 2026, BMC Medical Co., Ltd. (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. This corrective action was not reported to customers. O
What should I do if I have it?
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Which states are affected?
This recall is nationwide.
How do I identify the recalled product?
Look for: .
How serious is a Class II recall?
Class II means possible temporary or reversible harm.
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