FDA Device recall Z-2478-2026
Mito Red Light, Super Mobile
- FDA Device
- Class II
- ongoing
- Published 2026-06-24
On 2026-06-24 the FDA classified a Class II recall of Mito Red Light, Super Mobile by Mito Red Light, citing the near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2478-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-02-12 |
| Published | 2026-06-24 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Mito Red Light |
| Distribution | US |
Product
Mito Red Light, Super Mobile
Reason
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
Identifiers
| code_info | All Serial/Lot numbers/No UDI |
|---|
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-2478-2026%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.