Home › Device types › LYL
Accessories, Solution, Ultrasonic Cleaners For Lenses
FDA product code LYL · Class 2 · Ophthalmic
62
Registered devices
325
Adverse events
14
Recalls
22
510(k) clearances
Devices with this code
CVS HEALTH — WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDMeijer — MEIJER, INC.Amazon Basic Care — AMAZON.COM SERVICES LLCEquate — WAL-MART STORES, INC.Good Neighbor — Amerisourcebergen Drug CorporationPuriLens Plus Disinfecting System Cleaning Chamber — LIFESTYLE CO INC, THEPuriLens Plus Disinfecting System Exchange Kit — LIFESTYLE CO INC, THEWalgreens — WALGREEN CO.Walgreens — WALGREEN CO.Bausch + Lomb — Bausch & Lomb IncorporatedNexus Optical — NEXUS OPTICAL, INC.Bausch + Lomb — Bausch & Lomb IncorporatedNexus Optical — NEXUS OPTICAL, INC.Nexus Optical — NEXUS OPTICAL, INC.LEADER — Cardinal Health 110, Inc.Nexus Optical — NEXUS OPTICAL, INC.Bausch + Lomb — Bausch & Lomb IncorporatedMeijer — MEIJER, INC.Equate — WAL-MART STORES, INC.PuriLens Plus Disinfecting System 110V Adapter — LIFESTYLE CO INC, THEWalgreens — WALGREEN CO.Equate — WAL-MART STORES, INC.LEADER — Cardinal Health 110, Inc.Bausch + Lomb — Bausch & Lomb Incorporated
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-04 | Family Dollar Stores, Llc. | Products were stored outside of labeled temperature requirements. |
| 2014-09-25 | Bausch & Lomb Inc- Greenville Solutions Plant | Product lot did not meet the specification for its disinfectants at the time of manufacture. |
| 2014-04-21 | Bausch & Lomb Inc- Greenville Solutions Plant | Out of specification results for one of the two disinfectants. |
| 2011-06-30 | Bausch & Lomb Inc | Muti-purpose solution bottles, lot GC1107 were packaged in a carton that was marked with an incorrect lot code and expiration date. |
| 2010-12-22 | Bausch & Lomb Inc | There is a potential for some packages to not meet sterility requirements. |
| 2010-12-22 | Bausch & Lomb Inc | There is a potential for some packages to not meet sterility requirements. |
| 2010-02-03 | K C Pharmaceuticals Inc | The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free |
| 2010-02-03 | K C Pharmaceuticals Inc | The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free |
| 2010-02-03 | K C Pharmaceuticals Inc | The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free |
| 2010-02-03 | K C Pharmaceuticals Inc | The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free |
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