---
title: "Biofinity Toric Multifocal Contact Lens — FDA record Z-2166-2025 | Is It on Recall"
description: "Lens blisters may have an incomplete or leaking seal which may render them unsterile."
url: https://isitonrecall.com/recall/fda-device-z-2166-2025-biofinity-toric-multifocal-contact-lens/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Biofinity Toric Multifocal Contact Lens — FDA record Z-2166-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 16, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Biofinity Toric Multifocal Contact Lens
- **Reason**: Lens blisters may have an incomplete or leaking seal which may render them unsterile.
- **Classification**: Class II
- **Recalling firm**: CooperVision, Inc.
- **Quantity**: 827 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2166-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2166-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Carton Lot Numbers: RB0682365, RB0684301, RB0684305, RB0684311, RB0684313, RB0684317, RB0684321, RB0684325, RB0684335, RB0684506, RB0684575, RB0684582, RB0684653, RB0684657, RB0684659, RB0684663, RB0684664, RB0684667, RB0684668, RB0684669, RB0684670, RB0684673, RB0684674, RB0684676, RB0684682, RB0686359, RB0687092, RB0687368, RB0687370, RB0687547, RB0687582, RB0687586, RB0687665, RB0687693, RB0687797, RB0687800, RB0687801, RB0687802, RB0687803, RB0687807, RB0687812, RB0687822, RB0687893, RB0687897, RB0687904, RB0687908, RB0687910, RB0687922, RB0688105, RB0688107, RB0688109, RB0688113, RB0688117, RB0688121, RB0688128, RB0688130, RB0688145, RB0688147, RB0688151, RB0688163, RB0688170, RB0688174, RB0688269, RB0688298, RB0688300, RB0688305, RB0688307, RB0688320, RB0688322, RB0688343, RB0688492, RC1756323, RC1759660, RC1759663, RC1759931, RC1759947, RC1759965, RC1759967 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution - US Nationwide and the countries of Brazil, Canada, Honduras, and Mexico.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 30, 2025
- **Recall initiation date**: Jun 16, 2025
- **Center classification date**: Jul 23, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2166-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [CooperVision, Inc. records](https://isitonrecall.com/brand/coopervision-inc/)
