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Recall Observatory FDA recall evidence

Device product

Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System. Ophthalmic laser system use for correction of corneal refraction and ablation of the corneal surface. The system is composed of a laser generator which produces an excimer laser radiation of wavelength 193nm, a beam delivery unit, an optical system for observation, a gas system and a computer for system control.

Z-1494-2017

February 01, 2017

Class II

Product summary

Firm
Nidek Inc
Event
Event 76376
Status
Terminated
Classification
Class II
Quantity
29
Official record key
device-enforcement:Z-1494-2017

Official wording

Reason: During treatment planning, the procedure was programmed with an unintended (wrong) correction.

Code information: Software version 1.11 and 1.12. Serial numbers of Affected devices: MNE0009; NVE0002; OH00295; NC00185; CAE0016; COE0008; MI00131; GA00241; CAE0007; VAE0004; MI00131; CAE0031; AZ00167; COE0011; CA00561; PAE0003; TN00168; MNE0009; WA00246; CAE0047; OHE0005; WAE0008; MI00244; NY00473; CAE0007; WAE0008; NVE0002; WA00233; CAE0016.

Distribution pattern: Nationwide Distribution to MN, NV, OH, NC, CA, CO, CA, GA, VA, MI, AZ, PA, TN, WA, TX, NY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    During treatment planning, the procedure was programmed with an unintended (wrong) correction.