# FDA recall Z-1131-2019

> **Johnson & Johnson Vision Care, Inc.** · Class II · device recall initiated 2019-03-11.

## Product

ACUVUE OASYS for ASTIGMATISM brand contact lenses, Base Curve 8.6 Refractive Power -1.00D, -1.25D x 100, 6 pack.

## Reason for recall

One lot of ACUVUE OASYS¿ for ASTIGMATISM Brand Contact lenses has the potential for a limited number of individual contact lens packages to have an incomplete packaging seal.

## Distribution

Distributed to California.

## Key facts

- **Recall number:** Z-1131-2019
- **Recalling firm:** Johnson & Johnson Vision Care, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-11
- **Report date:** 2019-04-17
- **Termination date:** 2021-12-06

- **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-1131-2019

## Citation

> AI Analytics. FDA recall Z-1131-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1131-2019. Source: US FDA. Licensed CC0.

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