# FDA recall Z-0518-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-11-04.

## Product

Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of the human body.  Site~Rite 8 Ultrasound System, Catalog No.9770500  Refurbished, Site~Rite¿ 8 System, Catalog No.9770500R  Site~Rite 8 Ultrasound System, Catalog No.9770501  Refurbished Site~Rite¿ 8 System,Catalog No.9770501R  Site~Rite 8 Ultrasound System, Catalog No. 9770550  Site~Rite 8 Ultrasound System, Catalog No. 9770552  Site~Rite 8 Ultrasound System, Catalog No. 9770553  Site~Rite 8 Ultrasound System, Catalog No. 9770554  Site~Rite 8 Ultrasound System, Catalog No. 9770555  Site~Rite 8 Ultrasound System Console with Connector, Catalog No.: 9770600  Site~Rite 8 Ultrasound System Console with Connector, Refurbished, Catalog No: 9770600X  Site~Rite 8 Ultrasound System Console with Connector (Remanufactured)  Catalog No: 9770600Y

## Reason for recall

The indicator may show available charge when the battery is close to depletion. As a result, the Site~Rite 8 has the potential to abruptly shut down, without advance warning to the user, when running on battery power only

## Distribution

Nationwide  Foreign: UK, Belgium, Australia, Japan, Canada, Taiwan, Colombia, Chile, Philippines, Thailand, Brazil, Hong Kong, Chile, Argentina, Mexico, India, Singapore

## Key facts

- **Recall number:** Z-0518-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-11-04
- **Report date:** 2019-12-04
- **Termination date:** 2020-11-19

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0518-2020

## Citation

> AI Analytics. FDA recall Z-0518-2020. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-0518-2020. Source: US FDA. Licensed CC0.

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