medical MODERATE Updated 2026-08-26

Spectral Instruments Inc recalls Lago X

See all recalls from Spectral Instruments Inc →

Recalled Product

Lago X

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Hazard / Issue

Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All serial numbers.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Lago X →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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