# FDA recall Z-1163-2021

> **Johnson & Johnson Surgical Vision Inc** · Class II · device recall initiated 2021-01-27.

## Product

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

## Reason for recall

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

## Distribution

U.S. Nationwide distribution in the states of AL, AZ, CA, FL, GA, IL, LA, MI, MN, NC, NY, OH, PA, SC, TN, TX, UT and WA.

## Key facts

- **Recall number:** Z-1163-2021
- **Recalling firm:** Johnson & Johnson Surgical Vision Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-01-27
- **Report date:** 2021-03-10
- **Termination date:** 2022-11-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Ana, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1163-2021

## Citation

> AI Analytics. FDA recall Z-1163-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1163-2021. Source: US FDA. Licensed CC0.

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