Suntech Medical, Inc. Recalls

Overview of recall records associated with Suntech Medical, Inc., including dates, categories and classifications where available.

2recall records

Jul 1, 2020latest record date

Jan 22, 2020earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 1, 2020

Suntech Medical Oscar 2, Model 250 System recall — FDA Z-2429-2020

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.

Class IIFDA: TerminatedSuntech Medical, Inc.

Medical DeviceJan 22, 2020

Suntech Medical Model 250D Ambulatory Blood Pressure Monitor labeled under the following recall — FDA Z-0810-2020

The Bravo Mini (Model 250D), Agilis Mini (Model 250D), and NBP One (Model 250D) are being recalled because of a user safety issue when rechargeable batteries are misused in the product.

Class IIFDA: TerminatedSuntech Medical, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Suntech Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.