# FDA recall Z-1211-2018

> **Johnson & Johnson Vision Care, Inc.** · Class II · device recall initiated 2017-10-19.

## Product

1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses

## Reason for recall

Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.

## Distribution

Worldwide distribution.  US nationwide including Puerto Rico,   Korea, Czech Republic, China, Japan, Great Britain, Austria, Malaysia, Hong Kong, Russia, Taiwan, Singapore, India, and Brazil

## Key facts

- **Recall number:** Z-1211-2018
- **Recalling firm:** Johnson & Johnson Vision Care, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-19
- **Report date:** 2018-04-04
- **Termination date:** 2020-06-12

- **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-1211-2018

## Citation

> AI Analytics. FDA recall Z-1211-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1211-2018. Source: US FDA. Licensed CC0.

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