DeVilbiss Healthcare recalls 125 series iGO2 portable oxygen concentrators with unapproved adhesive in accumulator tank. Affected models include 125D and 125D-XB. Stop using immediately to avoid potential safety hazards.
An unapproved adhesive used to manufacture the accumulator tank sub assembly (a part of the patient gas pathway)
DeVilbiss Healthcare is recalling 125 series iGO2 portable oxygen concentrators due to an unapproved adhesive used in the accumulator tank subassembly. This could pose a safety risk if the device is used improperly. Affected units may need to be stopped or repaired.
The unapproved adhesive in the accumulator tank subassembly could cause leaks or failures in the patient gas pathway. This might lead to improper oxygen delivery or other safety issues if the device is used without proper maintenance.
Patients using portable oxygen concentrators for medical treatment are most at risk. Owners of the recalled 125D and 125D-XB models are affected.
Check for model numbers 125D or 125D-XB on the device. The serial numbers listed in the recall include D22829087DS through D22901207DS. The device is sold as a portable oxygen concentrator for supplemental oxygen administration.
Discontinue use of the device until it is repaired or replaced.
Reach out to DeVilbiss Healthcare for repair instructions or replacement options.
The affected models are 125D and 125D-XB with specific serial numbers listed in the recall notice.
The recall states an unapproved adhesive could cause leaks or failures in the patient gas pathway, but the exact risk level is not specified.
Check the model number on your device and compare it to the listed 125D or 125D-XB models. Also, verify the serial number against the provided list.
We’ve drafted a message you can send DeVilbiss Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0229-2023 — DeVilbiss Healthcare DeVilbiss Healthcare Hello, I own a DeVilbiss Healthcare that is covered by recall Z-0229-2023 from DeVilbiss Healthcare. 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.
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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.
