3B Medical React Health PHOENIX 5L Oxygen Concentrator Recall: Quality Issues
3B Medical recalls Phoenix 5L Oxygen Concentrators with quality issues that may not meet internal specifications. Affected units have specific serial numbers and UDI codes.
Lower-risk recall
Devices which did not meet internal quality specifications were inadvertently distributed.
Contact the company
What happened, in plain English
3B Medical is recalling Phoenix 5L Oxygen Concentrators that did not meet internal quality specifications. This recall is due to potential distribution of devices that may not meet quality standards, though no injuries have been reported. Read more at govinfonow.com/recall/50050-3b-medical-react-health-phoenix-5l-oxygen-concentrator-recall-quality.
Source Summary by GovInfoNow · govinfonow.com/recall/50050-3b-medical-react-health-phoenix-5l-oxygen-concentrator-recall-quality · Updated August 10, 2026 · FDA enforcement record: FDA #Z-1815-2026
Cite this page
“3B Medical React Health PHOENIX 5L Oxygen Concentrator Recall: Quality Issues.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/50050-3b-medical-react-health-phoenix-5l-oxygen-concentrator-recall-quality. Based on FDA recall #Z-1815-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1815-2026%22&limit=1).
Why it’s dangerous
The devices may not meet internal quality specifications, which could lead to potential issues with performance or safety. However, the recall does not specify a mechanism for injury or harm in normal use.
Who’s affected
Oxygen concentrator users who own the Phoenix 5L model with the specific serial numbers listed in the recall. Most at risk are individuals using medical oxygen for respiratory support.
How to tell if you have this one
Check for the serial number MZJ5S713971 or MZJ5S714009 on the device. The recall includes specific UDI codes starting with 06934726614439-250623-MZJ5S713971 and 06934726614439-250623-MZJ5S714009.
- Brand
3B Medical- Category
Medical device
What to do — step by step
Check Device Serial Number
Look for the serial number MZJ5S713971 or MZJ5S714009 on the oxygen concentrator.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-1815-2026 (February 4, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1815-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 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.