Collamer Ultraviolet Absorbing Posterior Chamber Intraocular Lens CQ2015A (UDI 00841542101936)Recalls & reported problems
Staar Surgical Company · Diopter: 17.5; 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 00841542101936), received between Nov 1, 2018 and Nov 1, 2018 — classified as 1 malfunction.
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
- No Apparent Adverse Event1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 1, 2018No Apparent Adverse Event; No Apparent Adverse Event
THE REPORTER INDICATED THAT A HAPTIC OF A CQ2015A, +17.5 DIOPTER, INTRAOCULAR LENS BENT DURING LOADING ON (B)(6) 2018 WITH NO PAITENT CONTACT. BACKUP LENS WAS IMPLANTED. THE PROBLEM RESOLVED.
Patient problems: No Patient Involvement
MAUDE report 8028718 ↗
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 · TerminatednanoFLEX 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 · TerminatedAfinity 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 · TerminatedBrand 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 · TerminatedSTAAR Surgical Intra Occular Lens, Collamer.
- Z-0539-04 · Feb 9, 2004 · TerminatedCollamer UV One-Piece IntraOcular Lens. Models 4205BF and 4204BF
Other Intraocular Lens devices
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens146 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens145 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens144 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens139 reports
- TECNIS SIMPLICITY DIB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens1 recall81 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens129 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens127 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens126 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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