OVERLOOKED

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Class IIOngoing

Spectral Instruments Inc recalls 2 products

Recall date · record updated Aug 26, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as fda mandated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Spectral Instruments Inc
Reason
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
United States.
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99631…

Products (2)

  1. Lago X

    Codes/lots: All serial numbers.Quantity: 40Recall no. Z-2939-2026Class II

  2. Ami HTX

    Codes/lots: All serial numbers.Quantity: 35Recall no. Z-2940-2026Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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