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Official Product Recall

This notice was issued by U.S. Food & Drug Administration (FDA).

FDA

BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect

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

This recall was published by U.S. Food & Drug Administration (FDA). View the full official notice for complete details, affected product codes, and what to do next.

View full recall notice

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What should I do?

  • 1.Stop using the product immediately if you have it.
  • 2.Check the full recall notice for affected batch numbers, UPCs, or model numbers.
  • 3.Follow the instructions in the recall notice for returns, replacements, or disposal.
  • 4.If you have health concerns after using the product, contact your GP or call NHS 111.
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Recall: Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76