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Collamer Ultraviolet Absorbing Posterior Chamber Intraocular Lens CQ2015A (UDI 00841542101905)Recalls & reported problems

Staar Surgical Company · Diopter: 16.0; Aspheric; Three Piece · Class 3 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841542101905), received between Oct 16, 2017 and Oct 16, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (1 report).

5 other recalls cover devices cleared under the same FDA submission (P990013); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Device Operates Differently Than Expected1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 16, 2017Device Operates Differently Than Expected; Device Operates Differently Than Expected

    THE REPORTER INDICATED THAT THE SURGEON ATTEMPTED TO IMPLANTED A CQ2015A, +16.0 DIOPTER, COLLAMER LENS IN THE PATIENT'S LEFT EYE (OS). AS THE SURGEON WAS LOADING THE LENS, HE WAS UNABLE TO GET IT IN THE INJECTOR. THERE WAS NO PATIENT CONTACT WITH THE LENS. HE DECIDED TO USE AND IMPLANT A BACK-UP LENS. THE PATIENT IS CURRENTLY FINE.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 6952442 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P990013. One submission often covers many models, so check the product and lot details in each record.

  • Z-1746-2013 · Jun 10, 2013 · Terminated
    nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by cataract extraction. The IOL is to be implante
  • Z-1747-2013 · Jun 10, 2013 · Terminated
    Afinity CQ2015A Intraocular Lens The visual correction of aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by cataract extraction.
  • Z-2706-2011 · May 20, 2011 · Terminated
    Brand Name STAAR Surgical Collamer Ultraviolet-Absorbing Posterior Chamber Single Piece Foldable Intraocular Lens Common Names Collamer single piece IOL Collamer plate haptic IOL
  • Z-1037-04 · Jun 17, 2004 · Terminated
    STAAR Surgical Intra Occular Lens, Collamer.
  • Z-0539-04 · Feb 9, 2004 · Terminated
    Collamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF

Other Intraocular Lens devices

All Intraocular Lens devices →

Sources and updates

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