Omron 10 Series Connected Upper Arm Blood Pressure Monitor BP7450Recalls & reported problems
Omron Healthcare, Inc. · Upper arm blood pressure monitor with Bluetooth connectivity, 2 users and 100 readings per user featuring TruRead. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00073796267452), received between Mar 30, 2021 and Apr 1, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Flare or Flash” (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
Device problems
- Flare or Flash2
- Smoking2
- Fire1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 1, 2021Smoking; Flare or Flash; Smoking; Flare or Flash
CONSUMER REPORTED THAT THE AC ADAPTER IS ON FIRE. THE AC ADAPTER SPARKING AND FLAMES COMING FROM THE SIDE OF THE UNIT WITH A BURNING SMELL. IT WAS NOT SPARKING OR FIRE FROM THE WALL SOCKET; JUST THE UNIT. THE UNIT DOES NOT TURN ON NOW WITH JUST BATTERIES. CONSUMER CHANGED THE BATTERIES AND NO POWER WITH NEW BATTERIES. CONSUMER STATED THERE WAS NO PROPERTY DAMAGE. HE PULLED THE PLUG OUT OF THE WALL AND THEN OUT OF THE UNIT. HE IS USING THE ORIGINAL AC ADAPTER WITH THE UNIT AND VERIFIED THAT AC ADAPTER PART NUMBER WAS HEM-ADPTW5. PER CONSUMER, THE UNIT THE UNIT WAS PLUGGED INTO THE OUT LET ON MARCH 17TH AND THIS ISSUE HAPPENED ON MARCH 22ND. THE UNIT WAS ON KITCHEN COUNTER. CONSUMER STATED FIRE DEPART WAS NOT CALLED. OMRON CUSTOMER SERVICE REPRESENTATIVE SENT POSTAGE PAID LABEL AND ADVISED CONSUMER TO RETURN THE UNIT THE UNIT USING POSTAGE PAID LABEL FOR FURTHER INVESTIGATION. DURING FOLLOW-UP CALL, CONSUMER STATED THE UNIT CAUGHT ON FIRE AND THIS HAPPENED ON MARCH 22ND. THEY SMELT SOMETHING BURNING AND STATED SEARCHING IN THE KITCHEN TO FIND WHERE THE SMELL WAS COMING FROM. IT SMELT LIKE BURNT PLASTIC. THE UNIT WAS ACTUALLY ON FIRE. HE USED THE TOWELS TO PUT THE FIRE OUT. THE FIRE W
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11600998 ↗MalfunctionMar 30, 2021Fire; Smoking; Flare or Flash; Fire; Smoking; Flare or Flash
CONSUMER REPORTED THAT THE AC ADAPTER IS ON FIRE. THE AC ADAPTER SPARKING AND FLAMES COMING FROM THE SIDE OF THE UNIT WITH A BURNING SMELL. IT WAS NOT SPARKING OR FIRE FROM THE WALL SOCKET; JUST THE UNIT. THE UNIT DOES NOT TURN ON NOW WITH JUST BATTERIES. CONSUMER CHANGED THE BATTERIES AND NO POWER WITH NEW BATTERIES. CONSUMER STATED THERE WAS NO PROPERTY DAMAGE. HE PULLED THE PLUG OUT OF THE WALL AND THEN OUT OF THE UNIT. HE IS USING THE ORIGINAL AC ADAPTER WITH THE UNIT AND VERIFIED THAT AC ADAPTER PART NUMBER WAS HEM-ADPTW5. PER CONSUMER, THE UNIT THE UNIT WAS PLUGGED INTO THE OUT LET ON MARCH 17TH AND THIS ISSUE HAPPENED ON MARCH 22ND. THE UNIT WAS ON KITCHEN COUNTER. CONSUMER STATED FIRE DEPART WAS NOT CALLED. OMRON CUSTOMER SERVICE REPRESENTATIVE SENT POSTAGE PAID LABEL AND ADVISED CONSUMER TO RETURN THE UNIT THE UNIT USING POSTAGE PAID LABEL FOR FURTHER INVESTIGATION. DURING FOLLOW-UP CALL, CONSUMER STATED THE UNIT CAUGHT ON FIRE AND THIS HAPPENED ON MARCH 22ND. THEY SMELT SOMETHING BURNING AND STATED SEARCHING IN THE KITCHEN TO FIND WHERE THE SMELL WAS COMING FROM. IT SMELT LIKE BURNT PLASTIC. THE UNIT WAS ACTUALLY ON FIRE. HE USED THE TOWELS TO PUT THE FIRE OUT. THE FIRE W
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11592673 ↗
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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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