Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

TECNIS Toric 1-Piece IOL Recalled by Johnson & Johnson Surgical Vision Inc Due to Due to the release of nonconforming Intraocular Lenses...

Date: January 27, 2021
Company: Johnson & Johnson Surgical Vision Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Johnson & Johnson Surgical Vision Inc directly.

Affected Products

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

Quantity: 27 lenses

Why Was This Recalled?

Due to the release of nonconforming Intraocular Lenses (IOLs).

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Johnson & Johnson Surgical Vision Inc

Johnson & Johnson Surgical Vision Inc has 7 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report