PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 19, 2025 Initiated: October 7, 2025 #Z-0481-2026

Product Description

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

Reason for Recall

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.

Details

Recalling Firm
Philips Respironics, Inc.
Units Affected
56 units (55 US, 1 OUS)
Distribution
US Nationwide distribution in the states of GA, ID, KY, NJ, NY and the country of Canada.
Location
Murrysville, PA

Frequently Asked Questions

What product was recalled?
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. Recalled by Philips Respironics, Inc.. Units affected: 56 units (55 US, 1 OUS).
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 19, 2025. Severity: Moderate. Recall number: Z-0481-2026.