Southmedic OxyMask O2 Adult REF OM-112: Oxygen tubing may disconnect

Take action

Contact the company & request your remedy

Recalling firmSouthmedic, Inc.50 Alliance Blvd, N/A · Barrie, N/A N/A

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Southmedic is recalling OxyMask O2 Adult REF OM-1125-14 because the oxygen tubing might disconnect from the mask, leading to insufficient oxygen delivery for patients. This could cause harm if the device stops working during use.

Why it’s dangerous

The oxygen tubing can become loose or disconnect from the mask during use. This causes the device to stop working, which may lead to inadequate oxygen delivery to patients who need it.

Who’s affected

Patients using the OxyMask O2 Adult for medical oxygen therapy are affected. Those with respiratory conditions requiring continuous oxygen delivery are at higher risk.

How to tell if you have this one

Check for the model number OM-1125-14 on the device. The product was sold with lot number W73887.

Brand
Southmedic
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device
Look for the model number OM-1125-14 on the device or packaging.

✎ GovInfoNow

Questions people ask

Is this product dangerous?

Yes, the oxygen tubing may disconnect, causing inadequate oxygen delivery to patients.

How can I tell if I have the recalled product?

Check for model number OM-1125-14 on the device or packaging. The product was sold with lot number W73887.

What should I do if I have this product?

The recall record does not specify a remedy, so contact Southmedic directly for guidance.

Take action

Contact Southmedic

We’ve drafted a message you can send Southmedic to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2141-2021 — Southmedic Southmedic

Hello,

I own a Southmedic that is covered by recall Z-2141-2021 from Southmedic.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-2141-2021 (May 25, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2141-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Southmedic, Inc. recalls OxyMask O2 Adult REF OM-1125-14

Use caution until it’s fixed