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SimplyGo Mini recallZ-0481-2026 · Philips Respironics, Inc. · initiated Oct 7, 2025

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Philips Respironics, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

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.

FDA root cause category: Nonconforming Material/Component

What the company is doing

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.

Recall details

Recall number
Z-0481-2026
Status
Open, Classified
Initiated by the company
Oct 7, 2025
Posted by the FDA
Nov 7, 2025
Recalling firm
Philips Respironics, Inc.
Quantity
56 units (55 US, 1 OUS)
Product code
CAW
Distribution
US Nationwide distribution in the states of GA, ID, KY, NJ, NY and the country of Canada.

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

Code information (models, lots, serial numbers)

Show the full code information (1k characters)

Product Code: 1116816; UDI-DI: 00606959032385; Serial Numbers: 2438V115830, 2438V115960, 2438V116033, 2438V115899, 2438V115832, 2438V115964, 2438V116034, 2438V115837, 2438V115965, 2438V116040, 2438V115840, 2438V115967, 2438V116044, 2438V115842, 2438V115968, 2438V116045, 2438V115844, 2438V115970, 2438V116046, 2438V115878, 2438V115972, 2438V116047, 2438V115890, 2438V115973, 2438V116048, 2438V115894, 2438V115974, 2438V116049, 2438V115895, 2438V115980, 2438V116050, 2438V115896, 2438V115981, 2438V116051, 2438V115897, 2438V115983, 2438V116052, 2438V115919, 2438V115984, 2438V116226, 2438V115937, 2438V115991, 2438V116229, 2438V115939, 2438V115992, 2438V116233, 2438V115942, 2438V115993, 2438V116249, 2438V115948, 2438V115994, 2438V116253, 2438V115957, 2438V115995, 2438V116258, 2438V117762;

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Sources and updates

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