Philips Respironics, Inc.: Device Recall

Recall #Z-0481-2026 · 10/07/2025

Class II: Risk

Recall Details

Recall Number
Z-0481-2026
Classification
Class II
Product Type
Device
Recalling Firm
Philips Respironics, Inc.
Status
Ongoing
Date Initiated
10/07/2025
Location
Murrysville, PA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
56 units (55 US, 1 OUS)

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.

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

Distribution Pattern

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

Other Recalls by Philips Respironics, Inc.

View all recalls by Philips Respironics, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.