# FDA recall Z-2277-2019

> **Suntech Medical, Inc.** · Class II · device recall initiated 2019-06-03.

## Product

SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20

## Reason for recall

Product is mislabeled. The label on the package is for a size #4 cuff, but the incorrect size #3 cuff was placed in the package.

## Distribution

Pakistan

## Key facts

- **Recall number:** Z-2277-2019
- **Recalling firm:** Suntech Medical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-03
- **Report date:** 2019-08-21
- **Termination date:** 2020-12-16

- **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-2277-2019

## Citation

> AI Analytics. FDA recall Z-2277-2019. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-2277-2019. Source: US FDA. Licensed CC0.

---

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