# FDA recall Z-1744-2020

> **Johnson & Johnson Vision Care, Inc.** · Class II · device recall initiated 2017-12-18.

## Product

ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G. Base Curve 8.6, Refractive Power -3.00D-1.25/90.

## Reason for recall

Package integrity failure observed during routine shift package integrity testing at an external re-packager.

## Distribution

Nationwide US.

## Key facts

- **Recall number:** Z-1744-2020
- **Recalling firm:** Johnson & Johnson Vision Care, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-18
- **Report date:** 2020-04-29
- **Termination date:** 2020-06-10

- **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-1744-2020

## Citation

> AI Analytics. FDA recall Z-1744-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1744-2020. Source: US FDA. Licensed CC0.

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