Data Foundry

Medical device recalls 2026

BMC/REACTHEALTH Luna G3 APAP REF LG 3600 — Class I medical device recall Z-2979-2026

Ongoing recall by BMC Medical Co., Ltd., reported 2026-08-26, distributed in FL. Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse

Recall numberZ-2979-2026
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBMC Medical Co., Ltd., Beijing, China
Recall initiated2026-07-15
Classified2026-08-19
Reported by FDA2026-08-26
DistributedFL
Quantity20,160 units
UPC / GTIN / UDI-DI06948538363331, 06948538365892
Serial numbersA3124909049, A3124909156, A3124909235, A3124909266, A3124909335, A3124909364, A3124909373, A3124911095, A3124911104, A3124911116, A3124911147, A3124911157, A3124911207, A3124911245, A3124911307, A3124911329, A3124911369, A3124911411, A3124912002, A3124912014, A3124912033, A3124912036, A3124912039, A3124912059, A3124912070 and 475 more
Model numbers3600

Product

BMC/REACTHEALTH Luna G3 APAP REF LG 3600

Reason for recall

Retroactive reporting for 2024 rework conducted at the 3B/React Health warehouse

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2979-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.