Electronic Blood Pressure Monitor JPD-900WRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06951740514514), received between Feb 19, 2019 and Feb 19, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 19, 2019Incorrect, Inadequate or Imprecise Result or Readings

  I USED AN AUTOMATIC WRIST BP CUFF MADE BY DRKEA AFTER COMING HOME FROM A SURGERY WITH A BLOOD LOSS OF 900CC¿S, A LOW RBC, LOW BP AND SERIOUS DEHYDRATION. I WAS TOLD TO WATCH MY BP AND DRINK AS MUCH AS POSSIBLE. IF MY BP STAYED LOW I WAS TO GO TO THE HOSPITAL ER IF I HAD SYMPTOMS, IE: DIZZINESS OR FAINTING OR STUMBLING. MY BP WAS CONSTANTLY 70¿S/50¿S. I WAS A BIT TIPSY AND DIZZY. AFTER 3 DAYS OF REHYDRATION, THE BP REMAINED VERY LOW. INSTEAD OF GOING TO THE HOSPITAL, BECAUSE I FELT FINE AT THAT POINT, I HAD A VISITING NURSE TO THE HOUSE AND THE NEXT DAY A PT VISIT. THEIR BP MEASUREMENT WITH A MANUAL ADULT ARM CUFF, MY BP WAS CONSISTENTLY 120/78. MY HUSBAND BOUGHT AN ADULT MANUAL ARM CUFF AND MY BP HAS BEEN FINE AT 120¿S/70¿S. I HAD NOT TAKEN ANY CARDIZEM FOR MY BP AS ORDERED TO RESUME WHEN BP STABILIZED AFTER REHYDRATION. NOT TO MENTION, MY HUSBAND TAKING A DAY OFF FROM WORK, LEAVING THE STAFF SHORT AND LOSING THAT DAY¿S PAY.

  Patient problems: Dizziness

  MAUDE report 8358941 ↗