Philips Respironics, Inc. recalls SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the S…

Recall date

October 7, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0481-2026

FDA classification

Class II

Brand / firm

Philips Respironics, Inc.

Sold / distributed

US Nationwide distribution in the states of GA, ID, KY, NJ, NY and the country of Canada.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What 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