# FDA recall Z-1076-2018

> **Genicon, Inc.** · Class II · device recall initiated 2017-07-19.

## Product

GENICON EZEE Retrieval, sterile, Rx only.

## Reason for recall

Plastic handle is breaking off of shaft inhibiting proper removal per Instructions for Use.

## Distribution

Distributed domestically to FL, IL, MI, TN, UT.      Distributed internationally to Dominican Republic, Ireland, Denmark, Spain, Switzerland, United Kingdom.

## Key facts

- **Recall number:** Z-1076-2018
- **Recalling firm:** Genicon, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-19
- **Report date:** 2018-03-28
- **Termination date:** 2020-05-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Winter Park, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1076-2018

## Citation

> AI Analytics. FDA recall Z-1076-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1076-2018. Source: US FDA. Licensed CC0.

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