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.
Devices which did not meet internal quality specifications were inadvertently distributed.
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.
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.
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.
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.
Look for the serial number MZJ5S713971 or MZJ5S714009 on the oxygen concentrator.
The devices did not meet internal quality specifications and were inadvertently distributed.
Check the serial number to see if it matches the recalled units; if so, contact 3B Medical for further instructions.
The recall does not specify a mechanism for injury or harm in normal use.
We’ve drafted a message you can send 3B Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1815-2026 — 3B Medical 3B Medical Hello, I own a 3B Medical that is covered by recall Z-1815-2026 from 3B Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.