Class II
FDA
BMC Luna G3 APAP recalled over See official notice
BMC Luna G3 APAP was recalled on September 7, 2026 because of see official notice. It is a Class II recall (possible temporary or reversible harm). Affected area: nationwide. Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
HazardSee official notice
Risk levelClass II
Affected areaNationwide
CategoryFood
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:
- Product as filed
- BMC Medical Co., Ltd. — Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect
The notice lists no UPC or lot code. Match the brand, product name and package size against the official FDA notice.
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.
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- BMC Medical Co., Ltd.
- Recall type
- Voluntary
- Quantity
- Distribution
- 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.
Compiled from the official FDA record by our data rules — how we build these pages. Spotted an error? Report it.
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