# FDA recall Z-1865-2021

> **Johnson & Johnson Vision Care, Inc.** · Class II · device recall initiated 2021-05-06.

## Product

ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear.  Base Curve 8.8,  Refractive Power -1.50

## Reason for recall

Potential that a limited number of individual contact lens packages have an incomplete packaging seal.

## Distribution

Worldwide Distribution.  US nationwide, Canada, Germany, Austria, Belgium, France, Luxemburg, Netherland, Portugal, Spain, Sweden, Switzerland, and Trinidad and Tobago.

## Key facts

- **Recall number:** Z-1865-2021
- **Recalling firm:** Johnson & Johnson Vision Care, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-05-06
- **Report date:** 2021-06-23
- **Termination date:** 2021-11-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Jacksonville, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1865-2021

## Citation

> AI Analytics. FDA recall Z-1865-2021. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1865-2021. Source: US FDA. Licensed CC0.

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