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Stop using now Medical device recall · FDA · Published December 9, 2024

Jiangsu Jumao X-Care O2C5L Oxygen Concentrator May Catch Fire During Use

Jiangsu Jumao X-Care recalls O2C5L oxygen concentrators due to fire risk. Units with serial numbers JA2311000001-JA2311003700 and JA2312000001-JA2312002080, and JA2401000001-JA2401000740 are affected. Contact for remedy.

🇺🇸 FDA recall #Z-0795-2025Medical deviceJiangsu Jumao X-Care ›
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Contact the company

Recalling firmJIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTDNo 36 Danyan Road, Lianxing Village · Danyang, China
✎ GovInfoNow plain-language explainer

Jiangsu Jumao X-Care is recalling O2C5L oxygen concentrators because they may melt or catch fire during use. This poses a fire hazard that could lead to injury or property damage if the device is used as intended. Read more at govinfonow.com/recall/53322-jiangsu-jumao-x-care-o2c5l-oxygen-concentrator-may-catch-fire.

Source Summary by GovInfoNow · govinfonow.com/recall/53322-jiangsu-jumao-x-care-o2c5l-oxygen-concentrator-may-catch-fire · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0795-2025

Cite this page

“Jiangsu Jumao X-Care O2C5L Oxygen Concentrator May Catch Fire During Use.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53322-jiangsu-jumao-x-care-o2c5l-oxygen-concentrator-may-catch-fire. Based on FDA recall #Z-0795-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0795-2025%22&limit=1).

Jiangsu Jumao X-Care Medical Equipment Co Ltd voluntarily recalled JMC5A Ni/TruAire-5 Oxygen Concentrators because they may melt or catch fire during use, according to the FDA. The agency announced the Class I recall on Dec. 9, 2024.

How to tell if you have it

  • Brand: Jiangsu Jumao X-Care
  • Product: JMC5A Ni/TruAire-5 Oxygen Concentrator
  • Model: O2C5L
  • UDI-DI: 00092237623152
  • Serial Number Ranges: JA2311000001-JA2311000740, JA2311000741-JA2311001480, JA2311001481-JA2311002220, JA2311002221-JA2311002960, JA2311002961-JA2311003700, JA2312000001-JA2312000740, JA2312000741-JA2312001480, JA2312001481-JA2312002080, JA2401000001-JA2401000740
  • Distribution: US: OH

The hazard

The oxygen concentrator may melt or catch on fire during use.

Context

GovInfoNow's records show other recent recalls of similar products include the 3B Medical React Health PHOENIX 5L Oxygen Concentrator (2026-02-04), the FUJIFILM FDR Visionary Suite CH-200 X-ray Device (2026-01-09), and the Ventec V+Pro Ventilator (2026-03-25).

How to tell if you have this one

Check the serial number on the device, which falls within the ranges JA2311000001-JA2311003700, JA2312000001-JA2312002080, or JA2401000001-JA2401000740. The product is sold under the brand Jiangsu Jumao X-Care.

  • Brand
    Jiangsu Jumao X-Care
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Stop Using It Now

    Immediately stop using the oxygen concentrator if it has a serial number in the affected ranges.

Where it went and when

Where it was distributed

Distributed in Ohio.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “US: OH” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Ohio.

Recall timeline

FDA published this recall 37 days after the firm started it.

1. Firm started the recall: Dec 9, 202412. FDA classified it Class I: Jan 3, 202523. Published in FDA’s Enforcement Report: Jan 15, 2025320242025
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What serial numbers are affected by this recall?

Serial numbers from JA2311000001 to JA2311003700, JA2312000001 to JA2312002080, and JA2401000001 to JA2401000740.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0795-2025 (December 9, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0795-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA