Bard® Extension Cord 153621Recalls & reported problems
C. R. Bard, Inc. · Bard® Extension Cord · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741045868), received between Oct 3, 2024 and Nov 10, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Erratic or Intermittent Display” (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
- Erratic or Intermittent Display3
- No Display/Image1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 10, 2025Erratic or Intermittent Display; Erratic or Intermittent Display
IT WAS REPORTED THAT THE HEALTH PROFESSIONAL HAD BEEN USING TEMPERATURE SENSING EXTENSION CABLE DISPLAY FOR ABOUT TWO WEEKS. IT WAS SHOWING STRANGE READINGS LIKE 32°C AND 34°C, MAKING IT UNRELIABLE. THE TEMPERATURE DISPLAY WAS SHOWING STRANGE READINGS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23513610 ↗MalfunctionNov 7, 2025No Display/Image; No Display/Image
IT WAS REPORTED THAT THE HEALTH PROFESSIONAL HAD BEEN USING TEMPERATURE SENSING EXTENSION CABLE DISPLAY FOR ABOUT A MONTH NOW AND THE TEMPERATURE WAS NOT DISPLAYED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23501362 ↗MalfunctionOct 3, 2024Erratic or Intermittent Display; Erratic or Intermittent Display
IT WAS REPORTED THAT THE TEMPERATURE SENSING EXTENSION CABLE DISPLAY SHOWED AN ABNORMAL TEMPERATURE VALUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20359560 ↗MalfunctionOct 3, 2024Erratic or Intermittent Display; Erratic or Intermittent Display
IT WAS REPORTED THAT THE BLADDER TEMPERATURE READING OF THE TEMPERATURE SENSING EXTENSION CABLE WAS ABNORMAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20359457 ↗
Other CATHETER, RETENTION TYPE, BALLOON devices
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- 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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