# FDA recall Z-1879-2018

> **CooperSurgical, Inc.** · Class II · device recall initiated 2018-03-12.

## Product

Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151

## Reason for recall

Products have been packaged with an incorrect product size.

## Distribution

CA, SC, WI, MI, NH, MD, OH, NJ, Australia, France, Spain

## Key facts

- **Recall number:** Z-1879-2018
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-12
- **Report date:** 2018-05-23
- **Termination date:** 2019-05-08

- **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-1879-2018

## Citation

> AI Analytics. FDA recall Z-1879-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1879-2018. Source: US FDA. Licensed CC0.

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