Philips Respironics, Inc. recalls SimplyGo Mini

Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output when in use in the device. If the fault occurs while the device is running on battery power, the SimplyGo Mini will shut down and stop providing oxygen to the user. This may happen at a temperature within the specified operating temperature range of the SimplyGo Mini.

SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600

On October 7, 2025 URGENT MEDICAL DEVICE RECALL letters were sent to customers. Actions for Distributors: Check inventory and place into quarantine any identified affected products. Complete and return the provided response form. Alert any customers who may have purchased affected products and work with them to return the affected product. A Philips representative will reach out regarding return and replacement of all affected product. Actions for patients: Check the serial numbers to verify if product affected by recall. If your product is affected, please discontinue use or the battery immediately. Contact your distributor and follow their instructions on how to receive a replacement battery and arrange for the return of the affected batteries in your possession. If the serial number on your battery kit does not match any of the affected serial numbers, then your battery is not affected by this issue and there is no need for any further action by you.

• FDA enforcement recordOfficial FDA database entry for Z-0481-2026
• FDA device classification · CAWOfficial FDA classification for this device type
• CFR regulation · 21 CFR 868.5440The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Philips Respironics, Inc.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.