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
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
- Bardex® All-Silicone Foley Catheter 165816C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON512 reports
- Bardex® Lubri-Sil® All-Silicone Foley Catheter 175816C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON476 reports
- Bardex® Lubri-Sil® I.C. All-Silicone Foley Catheter 1758SI16C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON1 death383 reports
- Bardex® Lubri-Sil® All-Silicone Foley Catheter 175812C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON234 reports
- Bardex® Lubri-Sil® All-Silicone Temp Sensing Foley Catheter 119216MC. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON167 reports
- Bardex® Lubri-Sil® All-Silicone Foley Catheter 175814C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON153 reports
- Bardex® All-Silicone Foley Catheter 165812C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON151 reports
- SureStep™ Foley Tray System Bard® Lubri-Sil® Foley Catheter Tray A942216C. R. Bard, Inc. · CATHETER, RETENTION TYPE, BALLOON2 recalls46 reports
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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