Spacelabs Ultraview SL Command Module Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Spacelabs Healthcare, Inc. is recalling 57 units of the Ultraview SL Command Module (model 91496) due to a manufacturing issue with an electrical leakage tester.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 26, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-device.
What Happened
Spacelabs Healthcare, Inc. initiated a voluntary recall of the Spacelabs Ultraview SL Command Module due to a manufacturing issue involving a malfunctioning electrical leakage tester.
Which Products Are Affected
The recall affects 57 units of the Brand Name: Spacelabs Ultraview SL Command Module, Product Name: SL Command Module, Model/Catalog Number: 91496. The devices were distributed worldwide, including US nationwide to GA, KS, MI, OH, SC, TX, WA and the country of Argentina. Specific serial numbers are listed in the recall notice.
What You Should Do
Consumers should refer to the recalling firm for further instructions regarding the affected devices.
Why This Matters
This Class II recall addresses a device defect that could lead to temporary or reversible adverse health consequences.
Source
FDA recall number Z-2052-2026, initiated March 26, 2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (894 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 26, 2026.
Frequently Asked Questions
Common questions about this FDA recall.