Johnson & Johnson Surgical Vision recalls
Johnson & Johnson Surgical Vision has 18 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 9 Sep 2026. 12 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is lead & heavy metals.
Total recalls18since 2018
Last 12 months1reported
Class I00% of total
Ongoing12latest 9 Sep 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 18 100%Class III 0 0%
Why johnson & johnson surgical vision is recalled
Product types
By year
Ongoing johnson & johnson surgical vision recalls
12 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Healon EndoCoat PRO recalled by Johnson & Johnson Surgical | Johnson & Johnson Surgical Vision | Other | Nationwide |
| Device | CLASS II | Johnson & Johnson Vision Reusable Laminar High Flow recalled | Johnson & Johnson Surgical Vision | Lead & Heavy Metals | Nationwide |
| Device | CLASS II | Tecnis Toric II OptiBlue IOL recalled by Johnson & Johnson Surgical | Johnson & Johnson Surgical Vision | Potency & Assay | Nationwide |
| Device | CLASS II | Tecnis Eyhance IOL recalled by Johnson & Johnson Surgical | Johnson & Johnson Surgical Vision | Sterility | Nationwide |
| Device | CLASS II | Tecnis Symfony, Extended Range of Vision IOL recalled | Johnson & Johnson Surgical Vision | Sterility | Nationwide |
| Device | CLASS II | Veritas Advanced Infusion Packs (Vrt-ai) recalled | Johnson & Johnson Surgical Vision | Lead & Heavy Metals | Nationwide |
All johnson & johnson surgical vision recalls, newest first
18 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.