FDA recall, , Moderate risk
Spacelabs Ultraview SL Command Module
The Spacelabs Ultraview SL Command Module has a manufacturing issue with its electrical leakage tester.
Summary by Recall Canary from the FDA notice
What happened
Spacelabs Healthcare, Inc. of Snoqualmie, Washington, is recalling the Spacelabs Ultraview SL Command Module, model 91496, due to a manufacturing issue involving a malfunctioning electrical leakage tester. The Command Module is the core of the Spacelabs patient monitoring system, providing processing power for basic physiologic parameters and inserting into the side of a patient monitor.
The recall began on March 26, 2026, and was added to the FDA's Enforcement Report on May 1, 2026, with distribution nationwide and in Argentina.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number matches.
SL Command Module
- Model number
- 91496
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide di GA, KS, MI, OH, SC, TX, WA and the country of ARGENTINA.
- Company
- Spacelabs Healthcare, Inc.Snoqualmie, Washington
- Hazard
- Manufacturing problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98722
- Recall number
- Z-2052-2026
All recalls from Spacelabs Healthcare, Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
