# FDA recall Z-0086-2023

> **Johnson & Johnson Surgical Vision, Inc.** · Class II · device recall initiated 2022-09-01.

## Product

Veritas Advanced Infusion Packs. Used in ophthalmic procedures.

## Reason for recall

As a result of returned product complaints for Veritas Phaco packs related to broken or cracked irrigation luer due to a manufacturing issue.

## Distribution

Worldwide Distribution. US states of AL, AR, AZ, CA, CO, DE, FL, GA, HI, IL IN, KY LA, MN, MO, MS, NC, NJ, NY, OH, TN, TX, UT, VA, and WA;    Australia, Azerbaijan, Belgium, Brazil, Canada, Denmark, Egypt, Estonia, Finland, France, Germany, Hong Kong, India, Iraq, Ireland, Italy, Japan, Jordan, Kuwait, Morocco, Netherlands, New Zealand, Oman, Poland, Portugal, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Turkey, United Arab Emirates, and United Kingdom

## Key facts

- **Recall number:** Z-0086-2023
- **Recalling firm:** Johnson & Johnson Surgical Vision, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-01
- **Report date:** 2022-10-19

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0086-2023

## Citation

> AI Analytics. FDA recall Z-0086-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0086-2023. Source: US FDA. Licensed CC0.

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