Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported August 4, 2021
OxyMask O2 Adult REF OM-1125-14
Potential for oxygen tubing to disconnect from mask or loosen. Disconnected tubing results in a loss of device function and use of the device could result in inappropriate or a…
Southmedic, Inc. recalled OxyMask O2 Adult REF OM-1125-14 - a moderate-severity action.
OxyMask O2 Adult REF OM-1125-14 was recalled by Southmedic, Inc. in August 4, 2021. Reason: Potential for oxygen tubing to disconnect from mask or loosen. Disconnected tubing results in a loss of de…. Check the official notice for the remedy. Verify recall #Z-2141-2021 with the FDA Devices before acting.
The recall
Southmedic, Inc. issued this moderate-severity FDA Devices recall-Potential for oxygen tubing to disconnect from mask or loosen. Disconnected tubing results in a loss of de….
- Moderate
- severity level
- Class II
- classification
- August 4, 2021
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2141-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2141-2021) was formally reported on August 4, 2021, with the manufacturer initiating the action on May 25, 2021. It is classified under Moderate severity (Class II), with a current status of Ongoing. Southmedic, Inc. is listed as the recalling firm, operating out of Barrie, N/A. Federal records list the affected scope as 160 cases (25 units per case) in U.S..
The documented reason for this recall is: Potential for oxygen tubing to disconnect from mask or loosen. Disconnected tubing results in a loss of device function and use of the device could result in inappropriate or a lack of oxygen delivery to the patient. Distribution data in the federal record shows the product reached: U.S.: IL O.U.S.: N/A. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
160 cases (25 units per case) in U.S.
Related Recalls
6
6 from same agency
Product description
OxyMask O2 Adult REF OM-1125-14
Reason for recall
Potential for oxygen tubing to disconnect from mask or loosen. Disconnected tubing results in a loss of device function and use of the device could result in inappropriate or a lack of oxygen delivery to the patient.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2141-2021 |
| Date reported | August 4, 2021 |
| Date initiated | May 25, 2021 |
| Recalling firm | Southmedic, Inc. |
| Firm location | Barrie, N/A |
| Affected scope | 160 cases (25 units per case) in U.S. |
| Distribution | U.S.: IL O.U.S.: N/A |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2141-2021) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
OxyMask O2 Adult REF OM-1125-14. Recalled by Southmedic, Inc.. Units affected: 160 cases (25 units per case) in U.S..
Why was this product recalled? ▼
Potential for oxygen tubing to disconnect from mask or loosen. Disconnected tubing results in a loss of device function and use of the device could result in inappropriate or a lack of oxygen delivery to the patient.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 4, 2021. Severity: Moderate. Recall number: Z-2141-2021.
Where was the recalled product distributed? ▼
Distribution: U.S.: IL O.U.S.: N/A.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2141-2021) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
FDA Devices Moderate
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Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
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FDA Devices Moderate
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Penumbra, Inc. · 2026-07-29
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SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System
Alphatec Spine, Inc. · 2026-07-29
Compare this recall with FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported August 4, 2021. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.