# FDA recall Z-1108-2022

> **CooperSurgical, Inc.** · Class II · device recall initiated 2022-04-01.

## Product

VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001    The VitriGuard device is a cryopreservation storage device composed of a stick and cap.

## Reason for recall

Products in this lot may have compromised barrier seals, introducing a risk to sterility.

## Distribution

Domestic distribution to AZ, CA, FL, IL, MI, MO, NY, OR, TX, and WV. No foreign distribution.

## Key facts

- **Recall number:** Z-1108-2022
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-01
- **Report date:** 2022-05-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Trumbull, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1108-2022

## Citation

> AI Analytics. FDA recall Z-1108-2022. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1108-2022. Source: US FDA. Licensed CC0.

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