Staar Surgical recalls
Staar Surgical appears in 14 official U.S. recall notices indexed by RecallRadar, most recently on 2023-12-13.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 14 |
|---|---|
| Published | 2013-07-24 to 2023-12-13 |
| By agency | FDA Device (14) |
| By classification | Class II (14) |
| By status | ongoing (11), terminated (3) |
| Distribution named in notices | AR, AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, US, UT, VA, WA, WI |
Recalls
- EVO +VISIAN Implantable Collamer Lens, REF: VICM5_13.7.Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_12.1. Phakic Toric Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO VISIAN Implantable Collamer Lens, REF: VICMO12.1. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO VISIAN Implantable Collamer Lens, REF: VICMO12.6. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO VISIAN Implantable Collamer Lens REF: VICMO13.2. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_12.6. Phakic Toric Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF: VICM5_12.6. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF:VTICM5_13.7. Phakic Toric Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_13.2. Phakic Toric Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - EVO+VISIAN Implantable Collamer Lens, REF: VICM5_13.2. Phakic Intraocular lens
FDA Device · Class II · 2023-12-13 · Staar Surgical
Reason: Their is a potential that intraocular implant devices may not meet specifications. - STAAR AQ Cartridge-FP, guide and delivery system for Intraocular lenses
FDA Device · Class II · 2016-06-22 · Staar Surgical
Reason: The STAAR AQ Cartridge-FP may malfunction and may crack during loading or delivery of the IOL (Intraocular Lenses). - Afinity CQ2015A Intraocular Lens The visual correction of aphakia in persons 60 years of age or older in whom a cataractous lens has been r…
FDA Device · Class II · 2013-07-24 · Staar Surgical
Reason: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and Afinity CQ2015A intraocular lenses due to the potential presence of glass particles in the storage vial. - nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by catara…
FDA Device · Class II · 2013-07-24 · Staar Surgical
Reason: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and Afinity CQ2015A intraocular lenses due to the potential presence of glass particles in the storage vial.