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QD Laser (6613) · RiskMitigated

Regulatory compliance issue involving MEOCHECK results and voluntary recall

First written in FY2025. 2 of 3 entries say "Mitigated", first in FY2026-H1. Latest entry: 2026-05-14.

3entries
2years
1from disclosures
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How it moved
ProgressHeldSoftenedWorseMaterialisedFY2025MitigatedFY2026-H1 – 2026-05-142025: 220252026: 12026
Same theme, other companies
Uncertainty in Obtaining Certifications and Approvals for Medical Devices and Responding to Healthcare SystemsA theme 11 companies write about · 13 as a headwind · 0 as a tailwind

The whole theme swung hardest in 2026: 3 of 7 companies on the "Worse" side.

1 other company's latest entry also says "Mitigated".

Ridges = years it wrote progress, valleys = years it wrote worse. Most hopeful companies at the back. Drag to turn, scroll to zoom, right-drag to pan. On a phone, two fingers turn and pinch to zoom; one finger scrolls the page.
Full recordFilings, disclosures and news, newest first
  1. 2026-05-14MitigatedEarningsSuggests it is closing out

    「Product recalls and software modifications have been completed, and the product has now made a fresh start as MEOCHECK NEO.」

    Following completion of the voluntary MEOCHECK recall and software modifications, the product made a fresh start as MEOCHECK NEO.
  2. FY2026-H1MitigatedAnnual report

    「As announced on 5 June 2025, regarding the eye self-check tool "MEOCHECK," we proceeded with a voluntary product recall after discovering that items for which the check results recommended seeking medical attention constituted diagnoses. As announced on 16 October 2025, we have completed the product recall and software modifications.」

    The regulatory compliance issue concerning MEOCHECK occurred, but the product recall and software modifications have been completed.
  3. FY2025MaterialisedAnnual report

    「It was discovered that the results of "MEOCHECK" and the "eye self-check service" constituted recommendations to seek medical attention, and we are proceeding with a voluntary product recall and software modifications.」

    It was confirmed that MEOCHECK's determinations constituted recommendations to seek medical attention, resulting in a voluntary product recall, software modifications and the suspension of sales activities.
Moved together

"Withdrawal of medical-device approval due to efficacy or safety issues" moved the same way as this thread, in the same document, in 3 of its 3 moves.

322222★123456
  1. ★This thread
  2. 1Withdrawal of medical-device approval due to efficacy or safety issues3×
  3. 2Loss burden associated with launching the laser eyewear business2×
  4. 3Expanding quantum-dot lasers into silicon photonics and LiDAR2×
  5. 4Expansion of Measurement Facilities and Enhancement of Manufacturing Equipment for the Laser Device Business2×
  6. 5Development of enabling technologies and monetization of intellectual property to realize smart glasses2×
  7. 6Continued product development and R&D2×

★ is this thread; numbers match the list above. The number on a line is how many documents both moved the same way in; lines between the other threads count the documents they moved together in too. Threads that move together often sit closer.

When this could move next
No upcoming earnings preview for QD Laser yet. It last moved in the Earnings of 2026-05-14: "Mitigated".
News
No news is linked to this thread yet. When an article touches it, it will appear here by date.
Regulatory compliance issue involving MEOCHECK results and voluntary recall | QD Laser,Inc. (6613) | Komori