United StatesBMC/REACTHEALTH Luna G3 APAP REF LG 3600 devices (UDI 06948538363331 and 06948538365892, Software Version G3-2.00.76; specific serial numbers listed by the firm) are affected. The recall was initiated for retroactive reporting related to 2024 rework conducted at the 3B/React Health warehouse; 20,160 units were distributed in the U.S. to Florida.
What's being recalled
BMC/REACTHEALTH Luna G3 APAP REF LG 3600
Recalling firm: BMC Medical Co., Ltd., Beijing, China.
How to identify it
UDI: 06948538363331; 06948538365892 Software Version: G3-2.00.76 Serial Numbers: A3124919140 A3124919145 A3124919181 A3124918105 A3124919105 A3124919148 A3124919131 A3124919151 A3124919130 A3124919147 A3124919153 A3124919126 A3124919149 A3124919144 A3124918225 A3124918400 A3124918379 A3124918407 A3124918228 A3124918390 A3124918398 A3124918268 A3124918260 A3124918341 A3124918259 A3124918285 A3124918251 A3124918464 A3124918255 A3124918257 A3124918261 A3124918172 A3124918267 A3124918266 A3124918280 A3124918212 A3124918269 A3124918382 A3124918271 A3124918130 A3124918246 A3124918525 A3124918282 A3124918528 A3124918294 A3124918362 A3124918529 A3124918358 A3124918374 A3124918516 A3124918364 A3124918509 A3124918511 A3124918366 A3124918385 A3124918372 A3124918376 A3124918263 A3124918512 A3124918380 A3124918287 A3124918085 A3124918300 A3124918297 A3124917180 A3124919172 A3124919058 A3124919054 A3124919116 A3124919057 A3124919189 A3124919112 A3124919115 A3124918327 A3124919100 A3124918197 A3124919120 A3124919191 A3124919186 A3124919118 A3124918115 A3124918317 A3124918429 A3124919137 A3124918153 A3124918207 A3124918069 A3124918323 A3124918023 A3124918136 A3124918070 A3124918081 A3124918134 A3124918051 A3124918114 A3124918283 A3124917222 A3124918182 A3124918030 A3124917146 A3124918037 A3124918180 A3124918185 A3124918169 A3124918042 A3124918183 A3124918056 A3124918166 A3124918038 A3124918163 A3124918448 A3124917327 A3124918160 A3124918444 A3124918124 A3124918441 A3124918107 A3124918256 A3124918119 A3124918128 A3124918450 A3124918447 A3124918123 A3124918112 A3124918431 A3124918293 A3124918440 A3124918428 A3124919087 A3124919008 A3124917075 A3124917345 A3124917393 A3124917129 A3124917305 A3124917059 A3124917277 A3124917070 A3124917103 A3124917061 A3124917308 A3124917385 A3124917376 A3124917392 A3124917156 A3124917133 A3124919185 A3124917055 A3124918032 A3124917144 A3124917391 A3124917151 A3124918168 A3124918325 A3124918164 A3124918120 A3124918439 A3124918044 A3124918449…
The hazard
Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US distribution to: FL OUS: None
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)