Well at Walgreens WGNBPA-950Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00311917183404), received between Feb 20, 2023 and Feb 20, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (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 20, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  HOMEDICS RECEVIED MDR REPORT # MW5114567 ON 2/7/2023. IN THE REPORT THE INDIVIDUAL WHO MADE THE REPORT AND WANTED TO REMAIN CONFIDENTIAL CLAIMED THE FOLLOWING: "THIS MACHINE GIVES ME LOW READINGS AND THEREFORE, I HAVE NOT TAKEN MY BLOOD PRESSURE MEDICATION IN WEEKS, AND I HAVE BEEN HAVING HEADACHES AND PRESSURE IN MY EYESIGHT." THE ALLEGED THIS WAS WITH MODEL #: WGNBPA-950. NOTE: THE INDIVIDUAL REPORTED THE MANUFACTUER AS "HOMEDICS GROUP CANADA". THIS IS NOT CONSISTENT AS THE MODEL IDENTIFIED (WGNBPA-950) IS SOLD EXCLUSIVELY TO WALGREENS IN THE US UNDER THEIR PRIVATE LABEL.

  Patient problems: Headache; Intracranial Pressure Increased

  MAUDE report 16405023 ↗