# FDA recall Z-2275-2020

> **Genicon, Inc.** · Class II · device recall initiated 2018-08-21.

## Product

Genicon Natura Model 210-005-152, 5mm diameter, 100mm length (two cannula, threaded) - Product Usage: The universal handle can be used as a  pistol grip  or like a traditional Trocar handle when using a scope.

## Reason for recall

There is potential for the plastic optical tip to become detached from the metal shaft.

## Distribution

US consignees in AL, DE, FL, GA, MO, NC, TN  Foreign consignees in Bahrain, Chile, Cyprus, Denmark, Dominican Republic, Egypt, Great Britain, Hong Kong, Ireland, Jordan, Kuwait, Lebanon, Pakistan, Singapore, South Africa, South Korea, and Thailand

## Key facts

- **Recall number:** Z-2275-2020
- **Recalling firm:** Genicon, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-08-21
- **Report date:** 2020-06-17

- **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-2275-2020

## Citation

> AI Analytics. FDA recall Z-2275-2020. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2275-2020. Source: US FDA. Licensed CC0.

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