FDA · recall · notice
FDA: BMC Medical recalls Luna G3 APAP devices due to firmware defect
BMC Medical Co., Ltd. recalled 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to a firmware defect. The recall was reported to the FDA on July 15, 2026, but was not reported to customers.
- Agency
- FDA
- Jurisdiction
- US-FDA
- Action type
- recall
- Severity
- notice — worth a prompt look
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- Recorded
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