Every recall we track for Johnson & Johnson Surgical Vision, Inc. — 17 in all — plus the complaints and injury reports the public filed about them.
Johnson & Johnson Surgical Vision recalls reusable laminar high flow irrigation sleeves (model OPOHF21L) due to a manufacturing defect that may cause insufficient irrigation flow during eye surgery, risking unstable anterior chamber.
Johnson & Johnson Surgical Vision recalls specific TECNIS Toric II OptiBlue IOL models due to an angle out of specification in the intraocular lens, which may affect alignment during cataract surgery.
Johnson & Johnson Surgical Vision recalls TECNIS Eyhance IOLs (REF: ICB00, STERILE.EO) due to potential unintended toric fiducial marks. Affected patients should contact the company for details.
Johnson & Johnson Surgical Vision recalls TECNIS Symfony Extended Range IOLs (REF: ZXR00) due to potential unintended toric fiducial marks. Affected units include specific serial numbers.
Johnson & Johnson Surgical Vision recalls VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF) due to potential priming cycle failure during surgery, which could cause longer procedures and temporary corneal swelling.
Johnson & Johnson Surgical Vision recalls single-use surgical packs with potential weld protrusion causing priming cycle failure and longer surgery times, risking corneal edema.
Johnson & Johnson Surgical Vision recalls Veritas Advanced Infusion Packs with specific lot numbers due to potential surgical delays from priming cycle failures. Affected units may cause longer procedures and temporary corneal swelling.
Johnson & Johnson Surgical Vision recalls FUSION Dual Pump Packs (REF: OPO73) due to potential surgical delays from pump failures. Affected units have specific UDI-DI/Lots numbers.
Johnson & Johnson Surgical Vision recalls Thermocoool Smarttouch SF Bi-Directional Navigation Catheters (REF: D-1348-05-S) due to potential cellulose fiber contamination that could cause irrigation failure or temperature issues during cardiac procedures.
Johnson & Johnson Surgical Vision recalls Veritas Advanced Infusion Packs used in eye surgery due to broken irrigation luer fittings. Affected units have specific lot numbers. Consumers should contact the company for details.
Johnson & Johnson Surgical Vision recalls sterile tray ring covers (OM27100:1) due to potential sterility barrier breach. Affected items contain a specific lot number range. Consumers should check their product details.
Johnson & Johnson Surgical Vision recalls TECNIS Eyhance IOLs with endotoxin levels exceeding safety limits. This nonconforming product was distributed in error during cataract surgery procedures.
Johnson & Johnson Surgical Vision recalls TECNIS Toric 1-Piece IOLs with model ZCT150 +23.5D SE 1.50D CYL due to nonconforming intraocular lenses that could pose risks during eye surgery.
Johnson & Johnson Surgical Vision recalls Healon GV PRO 0.85mL devices with specific models and lots due to difficulty removing from the eye, potentially causing increased pressure or ocular injury.
Johnson & Johnson Surgical Vision recalls disposable 25GA Vitrectomy Cutters (REF NGP0025) sold for surgery due to packaging error. A 20GA cutter may be in a 25GA package, risking surgical technique changes.
Johnson & Johnson Surgical Vision recalls expired Abbott TECNIS 1-Piece Aspheric Acrylic IOLs with TECNIS iTEC Preloaded Delivery System. Lenses manufactured before their expiration dates may cause vision issues.
Johnson & Johnson recalls OptiMedica Catalys Precision Laser Systems with specific software versions due to potential mismatch in plastic hemisphere cuts during daily alignment verification, affecting cataract surgery procedures.
