Theranica Bioelectronics recalls Nerivio Infinity devices with software version 4.1.2.0 and app version 7.28.0.11 due to potential smoke and odor during charging. Affected units may require replacement or repair.
Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor.
Theranica Bioelectronics is recalling Nerivio Infinity devices with specific software versions because they could overheat while charging, causing smoke and a bad smell. This hazard could lead to fire or injury if the device is used improperly.
The device's battery could overheat during charging due to a software issue, leading to smoke and a bad odor. This thermal runaway could potentially cause a fire if the device continues to charge without proper cooling.
Users of Nerivio Infinity devices with software version 4.1.2.0 and app version 7.28.0.11 are affected. People who charge these devices frequently are at higher risk of overheating.
Check for the model number FGD000100 on the device. The software version should be 4.1.2.0 and the app version 7.28.0.11. The serial number NI2544-0300673 is also associated with this recall.
Verify the software version is 4.1.2.0 and app version 7.28.0.11 by checking the device settings.
If the device shows signs of overheating, smoke, or a bad odor, stop using it immediately.
Software version 4.1.2.0 and app version 7.28.0.11 are affected.
Check for model number FGD000100, software version 4.1.2.0, app version 7.28.0.11, and serial number NI2544-0300673.
The recall record does not specify a remedy, so no fix is provided.
We’ve drafted a message you can send Theranica Bioelectronics to request your refund or repair — edit it as you like.
Subject: Recall Z-2855-2026 — Theranica Bioelectronics Theranica Bioelectronics Hello, I own a Theranica Bioelectronics that is covered by recall Z-2855-2026 from Theranica Bioelectronics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
