# FDA recall Z-2325-2017

> **Pentax of America Inc** · Class II · device recall initiated 2011-01-11.

## Product

Video Cytoscopes

## Reason for recall

This field action serves to retrospectively document the actions that were taken by Pentax  to correct the loose suction arms on eleven (11) models of endoscopes and to notify FDA of these actions taken in 2010-2011.

## Distribution

US Nationwide and Internationally

## Key facts

- **Recall number:** Z-2325-2017
- **Recalling firm:** Pentax of America Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2011-01-11
- **Report date:** 2017-06-21
- **Termination date:** 2018-03-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Montvale, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2325-2017

## Citation

> AI Analytics. FDA recall Z-2325-2017. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2325-2017. Source: US FDA. Licensed CC0.

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