# FDA recall Z-1227-2020

> **CooperVision Inc.** · Class II · device recall initiated 2020-01-13.

## Product

Coopervision Vertex Toric /2 Clear Toric-  Power -2.50 -0.75 /90  Soft (hydrophilic) Contact Lens (extended wear)

## Reason for recall

Incorrect power of lenses than the expected

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-1227-2020
- **Recalling firm:** CooperVision Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-01-13
- **Report date:** 2020-02-19
- **Termination date:** 2020-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Henrietta, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1227-2020

## Citation

> AI Analytics. FDA recall Z-1227-2020. Retrieved 2026-07-25 from https://api.ai-analytics.org/recall/Z-1227-2020. Source: US FDA. Licensed CC0.

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