Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported July 23, 2014
Spacelabs Healthcare Ultraview SL Multigas Module, Model 92518 (Software V1.00.00-09). Provides a means of monitoring a variety of gas concentrations and alert clinical personnel when the concentration of anesthetic agent(s), oxygen, carbon dioxide or nitrous oxide moves outside of user-defined limits.
With this software version, the Minimum Alveolar Concentration (MAC) value displayed is extremely high (20.1) and physiologically invalid.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Spacelabs Healthcare Inc recalled Spacelabs Healthcare Ultraview SL Multigas Module, Model 92518 (Software V1.00.00-09). P… - a moderate-severity action.
Spacelabs Healthcare Ultraview SL Multigas Module, Model 92518 (Software V1.00.00-09). P… was recalled by Spacelabs Healthcare Inc in July 23, 2014. Reason: With this software version, the Minimum Alveolar Concentration (MAC) value displayed is extremely high (20.1)…. Check the official notice for the remedy. Verify recall #Z-2077-2014 with the FDA Devices before acting.
The recall
Spacelabs Healthcare Inc issued this moderate-severity FDA Devices recall-With this software version, the Minimum Alveolar Concentration (MAC) value displayed is extremely high (20.1)….
- Moderate
- severity level
- 8 units
- affected scope
- Class II
- classification
- July 23, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2077-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2077-2014) was formally reported on July 23, 2014, with the manufacturer initiating the action on June 18, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Spacelabs Healthcare Inc is listed as the recalling firm, operating out of Snoqualmie, WA. Federal records list the affected scope as 8 units total (3 units in US).
The documented reason for this recall is: With this software version, the Minimum Alveolar Concentration (MAC) value displayed is extremely high (20.1) and physiologically invalid. Distribution data in the federal record shows the product reached: Worldwide Distribution - US in the state of Georgia and in the countries of : Malaysia, Paraguay, and France.. 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 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
8 units total (3 units in US)
Related Recalls
6
3 from same agency
Product description
Spacelabs Healthcare Ultraview SL Multigas Module, Model 92518 (Software V1.00.00-09). Provides a means of monitoring a variety of gas concentrations and alert clinical personnel when the concentration of anesthetic agent(s), oxygen, carbon dioxide or nitrous oxide moves outside of user-defined limits.
Reason for recall
With this software version, the Minimum Alveolar Concentration (MAC) value displayed is extremely high (20.1) and physiologically invalid.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2077-2014 |
| Date reported | July 23, 2014 |
| Date initiated | June 18, 2014 |
| Recalling firm | Spacelabs Healthcare Inc |
| Firm location | Snoqualmie, WA |
| Affected scope | 8 units total (3 units in US) |
| Distribution | Worldwide Distribution - US in the state of Georgia and in the countries of : Malaysia, Paraguay, and France. |
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-2077-2014) 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? ▼
Spacelabs Healthcare Ultraview SL Multigas Module, Model 92518 (Software V1.00.00-09). Provides a means of monitoring a variety of gas concentrations and alert clinical personnel when the concentration of anesthetic agent(s), oxygen, carbon dioxide or nitrous oxide moves outside of user-defined limits.. Recalled by Spacelabs Healthcare Inc. Units affected: 8 units total (3 units in US).
Why was this product recalled? ▼
With this software version, the Minimum Alveolar Concentration (MAC) value displayed is extremely high (20.1) and physiologically invalid.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 23, 2014. Severity: Moderate. Recall number: Z-2077-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - US in the state of Georgia and in the countries of : Malaysia, Paraguay, and France..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2077-2014) 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 23, 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.