# FDA recall Z-2429-2020

> **Suntech Medical, Inc.** · Class II · device recall initiated 2020-04-20.

## Product

Oscar 2, Model 250 System

## Reason for recall

The device display, when activated, can show an incorrect decimal point when the blood pressure reading is a three-digit number and the unit of measure is set for  mmHg.

## Distribution

Nationwide distribution to CA, CT, FL, IL, LA, MD, NC, NY, OH, PA, PR, SC, TN, TX, UT.      Worldwide distribution to Australia, Austria, Belgium, Bermuda, Brazil, Canada, Croatia, Czech Republic, Dominican Republic, Estonia, France, India, Ireland, Latvia, Lebanon, Morocco, Pakistan, Peru, Poland, Saudi Arabia, Singapore, South Africa, Spain, Taiwan, United Kingdom, Vietnam.

## Key facts

- **Recall number:** Z-2429-2020
- **Recalling firm:** Suntech Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-20
- **Report date:** 2020-07-01
- **Termination date:** 2023-06-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2429-2020

## Citation

> AI Analytics. FDA recall Z-2429-2020. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-2429-2020. Source: US FDA. Licensed CC0.

---

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