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YUWELL Electronic Blood Pressure Monitor

JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD. · Model YE8800AR · UDI-DI 06933257921634

DXN
1
510(k) clearances
7,287
Adverse events (16 deaths)
36
Recalls
428
Facilities

Description

YE8800AR is a rechargeable lithium battery-powered, automatic, noninvasive, wrist-worn blood pressure measuring system intended for over-the-counter (OTC) use. YE8800AR is designed for wrist circumference ranging from 13.5 cm to 19.5 cm. The systolic and diastolic blood pressures are measured using the oscillometric method, where the cuff is inflated with an air pump and deflates via an exhaust valve. During inflation, the cuff pressure is monitored, and pulse waveform data is extracted. The extracted pulse waveform data is then further analyzed by software which determines pulse rate, as well as systolic and diastolic blood pressure.

Recalls

DateFirmReason
2025-02-24PYRAMES INCSingle-use battery-powered blood pressure monitor, for use on neonates and infants, due to vibratory noise, may not adequately detect changes in blood pressure per specification. C
2024-08-30MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as
2024-08-30MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as
2024-08-30MEDLINE INDUSTRIES, LP - NorthfieldIt has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as
2024-03-26Baxter Healthcare CorporationBaxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical s
2024-03-26Baxter Healthcare CorporationBaxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical s
2024-03-26Baxter Healthcare CorporationBaxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical s
2024-02-26MEDLINE INDUSTRIES, LP - NorthfieldThe firm provided a set of specifications for the device, but some units of the device were manufactured non-compliant with the specifications. However, the firms Receiving Dept. a
2021-05-17Mediana Co., Ltd.In some cases the equipment fails to power up and/or key or button unresponsive or not working.
2021-04-22Welch Allyn IncPotential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.