Lago X
Spectral Instruments Inc · Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Open FDA's page for this record- Cfres ID
- 222029
- Product res number
- Z-2939-2026
- Event date initiated
- 2026-07-24
- Event date posted
- 2026-08-14
- Recall status
- Open, Classified
- Res event number
- 99631
- Product code
- RCE
- Product description
- Lago X
- Code info
- All serial numbers.
- Firm FEI number
- 3002679892
- Recalling firm
- Spectral Instruments Inc
- Address 1
- 420 N Bonita Ave
- City
- Tucson
- State
- AZ
- Postal code
- 85745-2747
- Reason for recall
- Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
- Root cause description
- Radiation Control for Health and Safety Act
- Action
- Customer notification letters dated August 21, 2023 and allows for scheduling of the software upgrade corrections.
- Product quantity
- 40
- Distribution pattern
- United States.
- Harmonized identifiers (openFDA)
- Device name
- Cabinet X-Ray, Industrial
- Medical specialty description
- Unknown
- Device class
- N