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# BMC Medical Recalls Sleep Apnea Machines
- URL: https://www.fdaweb.com/bmc-medical-recalls-sleep-apnea-machines/
- Published: 2026-09-10T12:00:00.000Z
- Updated: 2026-09-13T19:20:14.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5161757

BMC Medical has recalled (Class 1) its Luna G3 APAP (Model LG3600),an auto-adjusting positive airway pressure machine for treating obstructive sleep apnea, due to a firmware defect.

If affected devices operate simultaneously under high pressure, high respiratory rate, and high peak flow, an "Error" message on the device display is triggered, followed by automatic shutdown, resulting in a failure to deliver therapy. “The firmware defects could result in unintended serious adverse health consequences,” a [recall notice](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bmc-medical-co-ltd-recalls-luna-g3-apap-model-lg3600-firmware-g3-20076-due-firmware-defect?ref=fdaweb.com) says. To date, BMC has received no complaints or serious adverse reports associated with the issue.