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.

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 month

Severity split

Class I 0 0%Class II 18 100%Class III 0 0%

Why johnson & johnson surgical vision is recalled

By year

Ongoing johnson & johnson surgical vision recalls

12 active

All johnson & johnson surgical vision recalls, newest first

18 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIHealon EndoCoat PRO recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionOtherNationwide
DeviceCLASS IIJohnson & Johnson Vision Reusable Laminar High Flow recalledJohnson & Johnson Surgical VisionOtherNationwide
DeviceCLASS IITecnis Toric II OptiBlue IOL recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionPotency & AssayCA
DeviceCLASS IITecnis Eyhance IOL recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionOtherCA
DeviceCLASS IITecnis Symfony, Extended Range of Vision IOL recalledJohnson & Johnson Surgical VisionOtherCA
DeviceCLASS IIVeritas Advanced Infusion Packs (Vrt-ai) recalledJohnson & Johnson Surgical VisionDevice MalfunctionNationwide
DeviceCLASS IISingle-Use Packs recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionDevice Malfunction8 states
DeviceCLASS IIVeritas Advanced Infusion Packs recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionDevice Malfunction8 states
DeviceCLASS IIFusion Dual Pump Packs recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionDevice Malfunction8 states
DeviceCLASS IIThermocool Smarttouch SF Bi-Directional Navigation Catheter recalledJohnson & Johnson Surgical VisionParticulate MatterNationwide
DeviceCLASS IIVeritas Advanced Infusion Packs recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionDevice Malfunction24 states
DeviceCLASS IITray Ring Cover recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionSterilityNationwide
DeviceCLASS IITecnis Eyhance IOLs are permanent intraocular implants recalledJohnson & Johnson Surgical VisionPackaging DefectsNationwide
DeviceCLASS IITecnis Toric 1-Piece IOL recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionOtherNationwide
DeviceCLASS IIHealon GV PRO recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionOther46 states
DeviceCLASS IIDisposable Vitrectomy Cutter recalled by Johnson & Johnson SurgicalJohnson & Johnson Surgical VisionPackaging Defects10 states
DeviceCLASS IIAbbott Tecnis 1-Piece Aspheric Acrylic Iol recalledJohnson & Johnson Surgical VisionOtherNationwide
DeviceCLASS IIOptiMedica Catalys Precision Laser System, CE 0044 containing recalledJohnson & Johnson Surgical VisionForeign Material5 states

About 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.