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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

SimplyGo Mini Battery Kits Recalled for Potential Oxygen Supply Failure

Agency Publication Date: November 7, 2025
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Summary

Philips Respironics is recalling 56 SimplyGo Mini Standard Battery Kits used with the SimplyGo Mini Portable Oxygen Concentrator. A defective chip in these batteries can cause them to either fail to charge or suddenly lose power while the device is being used. If the battery fails, the device will shut down and stop providing oxygen to the user without warning.

Risk

The defective battery can cause the oxygen concentrator to stop functioning, cutting off the user's supplemental oxygen supply. This pose a serious risk of oxygen deprivation, especially if the user is reliant on the device for respiration and is unable to switch to a backup source quickly.

What You Should Do

  1. The recalled products are SimplyGo Mini Standard Battery Kits (Product code 1116816) sold as accessories for the SimplyGo Mini Portable Oxygen Concentrator.
  2. Identify if your battery is affected by checking the serial number on the device label. This recall involves 56 specific serial numbers including 2438V115830, 2438V115960, and 2438V116033. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled battery kit immediately.
  4. Return the product to the place of purchase for a refund or replacement, throw it away, or contact your healthcare provider or Philips Respironics for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider, or return the product to the place of purchase for a refund or replacement
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Stop using and throw the product away.

Affected Products

Product: SimplyGo Mini, Standard Battery Kit
Model / REF:
1116816
1113600
Serial Numbers (56):
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
Lot Numbers:
1116816
UDI:
00606959032385

Affected battery kits are sold as accessories for the SimplyGo Mini Portable Oxygen Concentrator.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97736
Status: Active
Manufacturer: Philips Respironics, Inc.
Sold By: Authorized medical equipment dealers; Direct distribution
Manufactured In: United States
Units Affected: 56 units (55 US, 1 OUS)
Distributed To: Georgia, Idaho, Kentucky, New Jersey, New York

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.