ReliOn BP3UP1-1ARLRecalls & reported problems
Wal-Mart Stores, Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00605388043863), received between Mar 7, 2018 and Mar 7, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Incorrect Or Inadequate Test Results” (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
Device problems
- Incorrect Or Inadequate Test Results1
Patient problems
- Fall1
- Loss of consciousness1
- Pain1
- Tooth Fracture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 7, 2018Incorrect Or Inadequate Test Results
(B)(6) CLAIMS THE BLOOD PRESSURE MONITOR CONSISTENTLY READ AROUND 160/98-102 FOR HIM ON MULTIPLE OCCASIONS. ON (B)(6) 2017, (B)(6) MEASURED HIS BLOOD PRESSURE WITH THE MONITOR AND OBTAINED A SIMILAR MEASUREMENT AGAIN. ON THE INSTRUCTION OF HIS DOCTOR, HE WAS TO TAKE AN EXTRA ½ DOSE OF HIS MEDICATION IF HIS READINGS WERE HIGH. (B)(6) TOOK THE EXTRA ½ DOSE AND CLAIMED HE FELT FINE. LATER THAT DAY, AROUND 7:30 PM (TIME OF PREVIOUS DRUG ADMINISTRATION NOT GIVEN), (B)(6) PREPARED SUPPER AND MOVED TO THE LIVING ROOM TO EAT. (B)(6) CLAIMS HE PLACED THE SUPPER PLATE DOWN ONTO A GLASS TOPPED TABLE (COFFEE TABLE/SIDE TABLE), AND THAT WAS THE LAST THING HE REMEMBERED UNTIL HE WOKE UP LYING ON THE FLOOR. (B)(6) BELIEVES HE WAS UNCONSCIOUS FOR APPROXIMATELY 20 MINUTES. IN FALLING, (B)(6) HAD ALSO BROKEN HIS GLASS TOPPED TABLE OF WHICH GAVE A SMALL CUT TO HIS SHIRT AND FINGER. (B)(6) ALSO HAD A SORE JAW AND SOME TEETH THAT FELT LOOSE AFTER HIS FALL THAT HE ATTRIBUTES TO POSSIBLY HITTING HIS JAW ON THE FLOOR OR TABLE WHEN FALLING. (B)(6) HAD NOT CLAIMED ANY ISSUE WITH EATING OR TEETH (OTHER THAN FEELING LOOSE) THE MULTIPLE TIMES HE DISCUSSED THE COMPLAINT WITH US SINCE THE INCIDENT. (B)(6) VISITE
Patient problems: Fall; Loss of consciousness; Pain; Tooth Fracture
MAUDE report 7322629 ↗
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- DTX(TM) PLUS DT-4812 682000Argon Critical Care Systems Singapore Pte. Ltd. · System, Measurement, Blood-Pressure, Non-Invasive86 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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