Has Johnson & Johnson Surgical Vision, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 8 total FDA actions tied to Johnson & Johnson Surgical Vision, Inc.: 0 warning letters, 8 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2024-01-24; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Johnson & Johnson Surgical Vision, Inc. — Class II recall: TECNIS Toric II OptiBlue IOL Models ZCW

Name: FDA Recall Record — Johnson & Johnson Surgical Vision, Inc.
Creator: Argus HQ
Published: 2024-01-24
License: https://argushq.ai/methodology

Event date: 2024-01-24 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: Z-0735-2024
Payload hash: c2b542989d37cc84096ab12e…

Summary

Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks. Status: Ongoing.

Entities

Johnson & Johnson Surgical Vision, Inc.

View source record ↗

Frequently asked questions

Has Johnson & Johnson Surgical Vision, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 8 total FDA actions tied to Johnson & Johnson Surgical Vision, Inc.: 0 warning letters, 8 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2024-01-24; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2024). Johnson & Johnson Surgical Vision, Inc. — Class II recall: TECNIS Toric II OptiBlue IOL Models ZCW. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-johnson-and-johnson-surgical-vision-inc-z-0735-2024

MLA

"Johnson & Johnson Surgical Vision, Inc. — Class II recall: TECNIS Toric II OptiBlue IOL Models ZCW." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-johnson-and-johnson-surgical-vision-inc-z-0735-2024.

Chicago

Argus HQ Research. "Johnson & Johnson Surgical Vision, Inc. — Class II recall: TECNIS Toric II OptiBlue IOL Models ZCW." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-johnson-and-johnson-surgical-vision-inc-z-0735-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_johnson_and_johnson_surgical_vision_inc_z_0735_2024_2024,
  title = {Johnson & Johnson Surgical Vision, Inc. — Class II recall: TECNIS Toric II OptiBlue IOL Models ZCW},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-johnson-and-johnson-surgical-vision-inc-z-0735-2024},
  note = {Accessed: July 23, 2026}
}

Informational only. Not legal, financial, or medical advice.