PlainRecalls

Johnson & Johnson Surgical Vision, Inc.

Compiled from official public sources by the publisher.

17 recalls on record · Latest: May 8, 2024

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Agency notice ledger

Federal filing book Johnson LIGHT-BOOK · SINGLE-AGENCY

#932 of 14,151 · 17 notices · 0.016% archive

  • BOOK 17 notices
  • RANK #932 of 14,151
  • SHARE 0.016% archive
  • AGENCY FDA Devices (17)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 8, 2024
  • PHOTO Actavis Inc

Nearest notice-volume peer: Actavis Inc (0 notice gap)

Johnson & Johnson Surgical Vision, Inc. accounts for about 0.016% of the 104,423-notice archive on 17 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Johnson compares to 14,151 recalling firms

Johnson & Johnson Surgical Vision, Inc. ranks 932nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Johnson vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

17 932nd of 14151 higher than 13,196 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Johnson in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Johnson & Johnson Surgical Vision, Inc. holds about 0.016% of archive notices alongside 17 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 8, 2024

Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The irrigation sleeve is a device intended to direct irrigation solution across the shaft of a phacoemulsification tip, allowing the solution to enter the eye during ocular surgery.
FDA Devices Moderate Jan 24, 2024

TECNIS Toric II OptiBlue IOL Models ZCW
FDA Devices Moderate Aug 9, 2023

VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
FDA Devices Moderate Aug 9, 2023

TECNIS Symfony, Extended Range of Vision IOL, REF: ZXR00, STERILE.EO, Rx Only
FDA Devices Moderate Aug 9, 2023

TECNIS Eyhance IOL, REF: ICB00, STERILE.EO, Rx Only
FDA Devices Moderate Feb 1, 2023

FUSION Dual Pump Packs, REF: OPO73
FDA Devices Moderate Feb 1, 2023

Veritas Advanced Infusion Packs, REF: VRT-AI
FDA Devices Moderate Feb 1, 2023

Single-Use Packs, REF: OPO80
FDA Devices Moderate Nov 9, 2022

THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation.
FDA Devices Moderate Oct 19, 2022

Veritas Advanced Infusion Packs. Used in ophthalmic procedures.
FDA Devices Moderate May 11, 2022

TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
FDA Devices Moderate Oct 13, 2021

TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS Simplicity Delivery System is designed as a single-use disposable preloaded modular cartridge that functions as both the primary packaging and as a sterile, disposable insertion system for delivering the IOL into the eye during cataract surgery.
FDA Devices Moderate Mar 10, 2021

TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.
FDA Devices Moderate Feb 5, 2020

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
FDA Devices Moderate Jul 10, 2019

Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one vitrectomy procedure. It is used to remove vitreous from the eye. It has been designed as a disposable (single use)
FDA Devices Moderate Nov 21, 2018

Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Preloaded Delivery System, Lens Model PCB00, Sterile, Rx - Product Usage: The lenses are indicated for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. These devices are intended to be placed in the capsular bag.
FDA Devices Moderate Oct 10, 2018

OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label for Serial Numbers: 44109015; 44106215; 44107315; and 44065613 label states "Manufactured for: OptiMedica Corporation 1310 Moffett Park Drive Sunnyvale, CA 94089 USA Product Label for Serial Numbers: 46120916; 46123116, 46124617; 46131418, and 46131618 label states "Manufactured for: OptiMedica Corporation 510 Cottonwood Drive Milpitas, CA 95035 USA The Catalys Precision Laser System is i

Johnson holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Ad-Tech Medical Instrument Corporation 17 Fhc, Inc. 17 Ge Healthcare It 17 Hitachi Medical Systems America Inc 17

Frequently Asked Questions

How many federal recall notices name Johnson? ▼
PlainRecalls indexes 17 distinct federal recall events naming Johnson & Johnson Surgical Vision, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Johnson sit among other recalling firms? ▼
Johnson & Johnson Surgical Vision, Inc. ranks #932 of 14,151 by distinct recall-event count among 14,151 firms in this archive (93rd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Johnson's notices? ▼
FDA Devices accounts for 17 of this firm's 17 indexed notices.
What product category dominates Johnson's filing book? ▼
Filings for Johnson & Johnson Surgical Vision, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Johnson & Johnson Surgical Vision, Inc.: 17 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Johnson & Johnson Surgical Vision, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026