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Suntech Medical Recalls
3 recalls on record · August 21, 2019 to July 1, 2020 · Medical Devices
Recalls by year
19
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 1, 2020Medical DevicesFDA
Suntech Medical, Inc. recalls Oscar 2, Model 250 System
Hazard: 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.
January 22, 2020Medical DevicesFDA
Suntech Medical, Inc. recalls Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part number 99-0233-00; Ag
Hazard: 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.
August 21, 2019Medical DevicesFDA
Suntech Medical, Inc. recalls SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20
Hazard: 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.