firmware
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Sleep Health
A recent recall of APAP devices has been classified as Class I after a firmware issue was found to cause unexpected shutdowns.
The United States Food and Drug Administration (FDA) has officially designated a recall of 20,160 Luna G3 APAP (Model LG3600)…
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Sleep Health
FDA Issues Warning Letter to BMC Medical Over Unapproved CPAP Modifications and Failure to Report Firmware Glitches
The United States Food and Drug Administration (FDA) has officially issued a formal warning letter to Beijing-based medical device manufacturer…
Read More » -
Sleep Health
FDA Warning Letter Issued to BMC Medical Over Unapproved CPAP Modifications and Failure to Report Firmware Safety Corrections
The United States Food and Drug Administration (FDA) has issued a formal warning letter to Beijing-based BMC Medical Co Ltd,…
Read More »
