Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported July 9, 2014
DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.
A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed into the unit, causing the unit serial number on LCD display to appea…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
DeVilbiss Healthcare LLC recalled DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA)… - a low-severity action.
DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA)… was recalled by DeVilbiss Healthcare LLC in July 9, 2014. Reason: A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed…. Check the official notice for the remedy. Verify recall #Z-1949-2014 with the FDA Devices before acting.
The recall
DeVilbiss Healthcare LLC issued this low-severity FDA Devices recall-A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed….
- Low
- severity level
- 2K units
- affected scope
- Class III
- classification
- July 9, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1949-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1949-2014) was formally reported on July 9, 2014, with the manufacturer initiating the action on May 13, 2014. It is classified under Low severity (Class III), with a current status of Terminated. DeVilbiss Healthcare LLC is listed as the recalling firm, operating out of Somerset, PA. Federal records list the affected scope as 1809.
The documented reason for this recall is: A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed into the unit, causing the unit serial number on LCD display to appear as "RUN-TEST". Distribution data in the federal record shows the product reached: Worldwide Distribution - USA (nationwide) and the countries of Colombia, Honduras, Iran, Thailand and Uruguay.. 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, 3 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 - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1809
Related Recalls
6
3 from same agency
Product description
DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.
Reason for recall
A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed into the unit, causing the unit serial number on LCD display to appear as "RUN-TEST".
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-1949-2014 |
| Date reported | July 9, 2014 |
| Date initiated | May 13, 2014 |
| Recalling firm | DeVilbiss Healthcare LLC |
| Firm location | Somerset, PA |
| Affected scope | 1809 |
| Distribution | Worldwide Distribution - USA (nationwide) and the countries of Colombia, Honduras, Iran, Thailand and Uruguay. |
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-1949-2014) 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? ▼
DeVilbiss Model DV5x Series CPAP units. For use in treating Obstructive Sleep Apnea (OSA) by means of application of positive air pressure. Used in home and clinical environments.. Recalled by DeVilbiss Healthcare LLC. Units affected: 1809.
Why was this product recalled? ▼
A limited number of DV5x Series CPAP units were manufactured and shipped without the serial number programmed into the unit, causing the unit serial number on LCD display to appear as "RUN-TEST".
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 9, 2014. Severity: Low. Recall number: Z-1949-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - USA (nationwide) and the countries of Colombia, Honduras, Iran, Thailand and Uruguay..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1949-2014) 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.
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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 July 9, 2014. 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 July 2026.