GARMIN BP707Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04719873310074), received between Oct 26, 2022 and Oct 26, 2022 — classified as 1 malfunction.

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.

• MalfunctionOct 26, 2022Incorrect, Inadequate or Imprecise Result or Readings

  USING THE GARMIN INDEX BPM MONITOR THAT I PURCHASED A FEW DAYS AGO, I HAVE BEEN CONSISTENTLY GETTING BLOOD PRESSURE READINGS THAT ARE 20+ POINTS OFF (HIGHER) ON THE SYSTOLIC AND 12-15 POINTS OFF ON THE DIASTOLIC, WHEN COMPARED TO A MANUAL READING AND OTHER DEVICES (OMRON). THE PRODUCT COMPLAINT DEPARTMENT AT GARMIN IS LESS THAN SATISFACTORY FOR MEDICAL DEVICE PRODUCT COMPLAINTS. IF YOU WANT FURTHER INFORMATION ON THEIR STANDARD OPERATING PROCEDURES, PLEASE CONTACT ME AT (B)(6). I AM SENDING THE UNIT BACK FOR A FULL REFUND, SO I WILL NOT HAVE THE PRODUCT IN MY POSSESSION PAST TODAY. HAD I NOT VERIFIED AND CALIBRATED THE GARMIN READINGS AS COMPARED TO OTHER DEVICES AND A MANUAL, I MAY HAVE BEEN ASKED TO ADJUST MY BP MEDS ACCORDINGLY, WHICH MAY HAVE RESULTED IN HYPOTENSION WITH HIGHER DOSES, OR MORE POTENT THERAPY. FDA SAFETY REPORT ID #(B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15680773 ↗