3 Series Blood Pressure Monitor BP710NRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00073796271046), received between Mar 15, 2023 and Mar 18, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “High Readings” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 18, 2023High Readings; High Readings

  THE CONSUMER STATED THAT HE WAS GETTING HIGH MEASUREMENTS FOR A YEAR AND HALF. HE HAD BEEN SELF-MEDICATING MORE MEDICATIONBASED ON THE HIGH READINGS THAT WERE ON THE UNIT, AND HE STATED THAT, AS A RESULT, HE HAD SEVERAL SIDE EFFECTS. HE CLAIMED THE MEDICATION AFFECTED HIS KIDNEYS AND THAT HIS BLOOD PRESSURE MONITOR MESSED HIM UP. HE DID NOT KNOW WHAT MEDICATION HE WAS TAKING EXTRA SINCE HIS WIFE GAVE HIM HIS MEDICATION. HE STATED HIS WIFE WOULD BASE HIS MEDICATION BASED ON WHAT THE DOCTOR WOULD RECOMMEND. HE MENTIONED THAT HE REMEMBERED THE MEDICATIONS ELIQUIS (BLOOD THINNER) AND METOPROLOL (BLOOD PRESSURE), BUT HE WAS NOT SURE WHAT MEDICATIONS HE WAS CURRENTLY TAKING. HIS DOCTOR HAD INCREASED MEDICATION AND CHANGED MEDICATIONS SEVERAL TIMES. HE SEEKED MEDICAL ATTENTION FOR THE LAST 2 YEARS EVERY 3-4 MONTHS FOR HIS KIDNEYS. THE MEDICAL ATTENTION INCLUDED CHECKING HIS BLOOD AND KIDNEYS. HE WAS NOT ADMITTED AT A HOSPITAL AS A RESULT OF THE COMPLAINT, BUT HE MENTIONED HE HAD PREVIOUSLY BEEN ADMITTED UNRELATED TO THIS COMPLAINT. HE DID NOT KNOW WHEN HE PURCHASED HIS UNIT. HIS ARM CIRCUMFERENCE WAS 12 INCHES. HE TOOK HIS READINGS WHILE SITTING WITH HIS ARM ON THE TABLE. HE USED THE CUFF

  Patient problems: Unspecified Heart Problem; Unspecified Kidney or Urinary Problem

  MAUDE report 16569792 ↗
• InjuryMar 15, 2023High Readings; High Readings

  THE CONSUMER STATED THAT HE WAS GETTING HIGH MEASUREMENTS FOR A YEAR AND HALF. HE HAD BEEN SELF-MEDICATING MORE MEDICATION BASED ON THE HIGH READINGS THAT WERE ON THE UNIT, AND HE STATED THAT, AS A RESULT, HE HAD SEVERAL SIDE EFFECTS. HE CLAIMED THE MEDICATION AFFECTED HIS KIDNEYS AND THAT HIS BLOOD PRESSURE MONITOR MESSED HIM UP. HE DID NOT KNOW WHAT MEDICATION HE WAS TAKING EXTRA SINCE HIS WIFE GAVE HIM HIS MEDICATION. HE STATED HIS WIFE WOULD BASE HIS MEDICATION BASED ON WHAT THE DOCTOR WOULD RECOMMEND. HE MENTIONED THAT HE REMEMBERED THE MEDICATIONS ELIQUIS (BLOOD THINNER) AND METOPROLOL (BLOOD PRESSURE), BUT HE WAS NOT SURE WHAT MEDICATIONS HE WAS CURRENTLY TAKING. HIS DOCTOR HAD INCREASED MEDICATION AND CHANGED MEDICATIONS SEVERAL TIMES. HE SEEKED MEDICAL ATTENTION FOR THE LAST 2 YEARS EVERY 3-4 MONTHS FOR HIS KIDNEYS. THE MEDICAL ATTENTION INCLUDED CHECKING HIS BLOOD AND KIDNEYS. HE WAS NOT ADMITTED AT A HOSPITAL AS A RESULT OF THE COMPLAINT, BUT HE MENTIONED HE HAD PREVIOUSLY BEEN ADMITTED UNRELATED TO THIS COMPLAINT. HE DID NOT KNOW WHEN HE PURCHASED HIS UNIT. HIS ARM CIRCUMFERENCE WAS 12 INCHES. HE TOOK HIS READINGS WHILE SITTING WITH HIS ARM ON THE TABLE. HE USED THE CUF

  Patient problems: Unspecified Heart Problem; Unspecified Kidney or Urinary Problem

  MAUDE report 16548193 ↗