# FDA recall Z-2742-2017

> **Pentax of America Inc** · Class II · device recall initiated 2017-04-13.

## Product

7245C, 7245C/E, 7245D  Computer Digital Video System    Product Usage:  The 7245C, 7245C/E and 7245D are used to electronically record, display, transfer, and store digital video data of behavior related to swallowing in the pharyngeal area for medical and pedagogical applications.

## Reason for recall

Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

## Distribution

Worldwide Distribution - US Nationwide

## Key facts

- **Recall number:** Z-2742-2017
- **Recalling firm:** Pentax of America Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-04-13
- **Report date:** 2017-07-26
- **Termination date:** 2019-03-22

- **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-2742-2017

## Citation

> AI Analytics. FDA recall Z-2742-2017. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2742-2017. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*