FDA Device recall Z-2979-2026
BMC/REACTHEALTH Luna G3 APAP REF LG 3600
- FDA Device
- Class I
- ongoing
- Published 2026-08-26
On 2026-08-26 the FDA classified a Class I recall of BMC/REACTHEALTH Luna G3 APAP REF LG 3600 by Bmc Medical, citing retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2979-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-07-15 |
| Published | 2026-08-26 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Bmc Medical |
| Distribution | FL |
Product
BMC/REACTHEALTH Luna G3 APAP REF LG 3600
Reason
Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse
Identifiers
| code_info | UDI: 06948538363331; 06948538365892 Software Version: G3-2.00.76 Serial Numbers: A3124919140 A3124919145 A3124919181 A…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 A31249 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2979-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.