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Bard® Dual Connector to Two Pin Plug, Monitor Cable 153624HMRecalls & reported problems

C. R. Bard, Inc. · Bard® Dual Connector to Two Pin Plug, Monitor Cable · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
8
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00801741045899), received between May 19, 2017 and Dec 29, 2025 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Break” (3 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.

Reports received per month

Nov 2023: 1 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 1 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break3
  • High Readings3
  • Overheating of Device2
  • Bent1
  • Material Fragmentation1
  • Material Twisted/Bent1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4
  • No Known Impact Or Consequence To Patient4
  • No Consequences Or Impact To Patient3

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 29, 2025Overheating of Device; Overheating of Device

    IT WAS REPORTED THAT ONE OUR END USERS EXPERIENCED A MALFUNCTION WHILE USING BARD#153624HM, THEY REPORTED THAT THEY USED THIS CORD TWICE AND, ON THE 2ND USE, THE PRONGS WERE BURNT. REQUESTED FOR CREDIT, REBILL AND REPLACEMENT CAN BE PROVIDED IN THIS INSTANCE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23913002 ↗
  • MalfunctionSep 25, 2024Overheating of Device; Overheating of Device

    IT WAS REPORTED THAT NEW EXTENSION CORD OF TEMPERATURE SENSING FOLEY CATHETER WAS USED FOR ABOUT 1 WEEK. THEY WERE NO LONGER WORKING, AND IT LOOKED FRIED WITH BLACK RESIDUE INSIDE OF THE PORT THAT CONNECTS TO PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20302009 ↗
  • MalfunctionNov 10, 2023Material Fragmentation; Material Fragmentation

    IT WAS REPORTED THAT THE BLACK TEMPERATURE CORD WAS FREQUENTLY BROKEN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18110428 ↗
  • MalfunctionAug 9, 2023Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED THAT THE TEMPERATURE SENSING EXTENSION CORD IN THE BOX WAS BENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17491025 ↗
  • MalfunctionMay 22, 2019Break; Break; High Readings

    IT WAS REPORTED THAT THE TEMPERATURE READING WAS 2-5 DEGREES HIGHER THAN IT SHOULD BE.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 8633891 ↗
  • MalfunctionMay 22, 2019Break; Break; High Readings

    IT WAS REPORTED THAT THE TEMPERATURE READING WAS 2-5 DEGREES HIGHER THAN IT SHOULD BE.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 8633669 ↗
  • MalfunctionMay 22, 2019Break; Break; High Readings

    IT WAS REPORTED THAT THE TEMPERATURE READING WAS 2-5 DEGREES HIGHER THAN IT SHOULD BE.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 8633305 ↗
  • MalfunctionMay 19, 2017Bent

    IT WAS REPORTED THAT THE PRONG WAS BENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6578723 ↗

Other CATHETER, RETENTION TYPE, BALLOON devices

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Sources and updates

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