Lago X Recall Issued by Spectral Instruments Inc
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Spectral Instruments Inc is recalling 40 units of the Lago X device in the United States due to a momentary absence of the On-Screen "X-Ray On" banner.
Reading this FDA recall beyond the headline
This notice was issued by FDA on September 9, 2026 and geographically references United States. The FDA classifies this as a Class II recall, with the stated reason "Momentary absence of On-Screen "X-Ray On" banner during run readiness check.", distributed united states.. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. 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, Devices.
What Happened
Spectral Instruments Inc initiated a recall of the Lago X device because of a momentary absence of the On-Screen "X-Ray On" banner during run readiness check.
Which Products Are Affected
The recall affects the Lago X device. All serial numbers are included. A total of 40 units were distributed in the United States. The recall number is Z-2939-2026.
What You Should Do
Consumers should follow guidance from the recalling firm or the FDA regarding the affected devices.
Why This Matters
This is a Class II recall involving a device distributed nationwide.
Source
FDA recall Z-2939-2026
Original source: FDA Official Notice ↗
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Comparable nationwide notices (length or severity timing) 8
Two cross-category peer sets, both computed from Areazine's own archive: notices with a similar body length, and notices near the same severity and agency date. These are drawn from other categories, not the same-feed Related list above.
Similar body length
Nearest notices by article body length (618 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to September 9, 2026.
Questions & Answers
Common questions about this FDA recall.