Johnson & Johnson Surgical Vision, Inc. recalls
Every recall we track for Johnson & Johnson Surgical Vision, Inc. — 18 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Johnson & Johnson Surgical Vision, Inc. peaked in 2022 (6); 18 since 2017.
All FDA recall records for Johnson & Johnson Surgical Vision, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 2 | 0 | 3 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 1 | 2 |
| 2022 | 0 | 1 | 4 | 1 | 6 |
| 2023 | 0 | 0 | 4 | 0 | 4 |
| 2024 | 0 | 1 | 0 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
What to do if you have a recalled Johnson & Johnson Surgical Vision, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Johnson & Johnson Surgical Vision, Inc. recalls
15 shown- Use cautionMedical device
Johnson & Johnson Surgical Vision, Inc. recalls HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:
Johnson & Johnson Surgical Vision recalls HEALON EndoCoat PRO and HEALON DUET PRO II products due to risk of corneal abrasion or eye damage if cannula is forced during cataract surgery.
Johnson & Johnson Surgical VisionJul 31, 2026 - Use cautionMedical device
Johnson & Johnson Surgical Vision, Inc. recalls Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The
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 VisionMar 14, 2024 - Lower riskMedical device
Johnson & Johnson Surgical Vision, Inc. recalls TECNIS Toric II OptiBlue IOL Models ZCW
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 VisionDec 12, 2023 - Lower riskMedical device
Johnson & Johnson Surgical Vision, Inc. recalls TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only
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 VisionJul 6, 2023 - Lower riskMedical device
Johnson & Johnson Surgical Vision, Inc. recalls VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
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 VisionMay 30, 2023 - Lower riskMedical device
Johnson & Johnson Surgical Vision, Inc. recalls FUSION Dual Pump Packs, REF: OPO73
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 VisionDec 7, 2022 - Lower riskMedical device
Johnson & Johnson Surgical Vision, Inc. recalls THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac
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 VisionSep 7, 2022 - Use cautionMedical device
Johnson & Johnson Surgical Vision, Inc. recalls Veritas Advanced Infusion Packs. Used in ophthalmic 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 VisionSep 1, 2022 - UnratedMedical device
Johnson & Johnson Surgical Vision Inc recalls TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
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 VisionApr 6, 2022 - Lower riskMedical device
Johnson & Johnson Surgical Vision Inc recalls TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS
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 VisionAug 6, 2021 - UnratedMedical device
Johnson & Johnson Surgical Vision Inc recalls TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the
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 VisionJan 27, 2021 - Use cautionMedical device
Johnson & Johnson Surgical Vision Inc recalls Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
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 VisionDec 3, 2019 - Lower riskMedical device
Johnson & Johnson Surgical Vision Inc recalls Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item
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 VisionSep 24, 2018 - Lower riskMedical device
Johnson & Johnson Surgical Vision Inc recalls Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Preloaded Delivery System, Lens Model PCB00, Sterile,
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 Surgical VisionJun 21, 2018 - Use cautionMedical device
Johnson & Johnson Surgical Vision Inc recalls OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label for Serial Numbers:
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.
OptiMedicaMay 9, 2018
Johnson & Johnson Surgical Vision, Inc. recall questions
How many recalls has Johnson & Johnson Surgical Vision, Inc. had?
18 recalls from Johnson & Johnson Surgical Vision, Inc. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Johnson & Johnson Surgical Vision, Inc. recall?
Johnson & Johnson Surgical Vision, Inc. recalls HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:, dated Jul 31, 2026. Every Johnson & Johnson Surgical Vision, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Johnson & Johnson Surgical Vision, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Johnson & Johnson Surgical Vision, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.