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Bard® Blakemore Esophageal-Nasogastric Tube 0092110Recalls & reported problems

C. R. Bard, Inc. · Bard® Blakemore Esophageal-Nasogastric Tube · Class 2

All models of Bard Blakemore Esophageal-Nasogastric Tube (3)

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

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741076817), received between Jan 13, 2026 and Jan 23, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Component Misassembled” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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: 0 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: 0 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: 0 reportsJan 2026: 3 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 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Apr 17, 2025Class IOpen, Classified

    Due to customer complaints, there is a potential for users to be unable to or find it difficult to remove the plastic plugs in order to inflate the gastric and/or esophageal balloons.

    Z-1757-2025 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Device problems

  • Component Misassembled1
  • Component Missing1
  • Insufficient Device Problem Information1
  • Nonstandard Device1
  • Separation Failure1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 23, 2026Nonstandard Device; Insufficient Device Problem Information

    IT WAS REPORTED THAT THE ENDO HAD EXPERIENCED ISSUES WITH THE 0092110 BLAKEMORE AND STATED THEY HAD BEEN UNABLE TO REMOVE THE PLASTIC PIECES FROM THE END. AT THAT POINT, IT WAS DISCOVERED THAT A POSSIBLE CONNECTOR HAD BEEN MISSING AND THAT EDUCATION WAS NEEDED. SUBSEQUENTLY, A LIST WAS SENT INDICATING THAT THE PRODUCT HAD ACTUALLY BEEN DISCONTINUED, AND THEY HAD PROVIDED THE 0092300 AS THE REPLACEMENT TO ORDER INSTEAD. HOWEVER, IT HAD NOT YET BEEN RECEIVED, AND THE PURCHASE ORDER HAD SOMEHOW BEEN CLOSED. IT WAS UNCLEAR WHETHER THIS OCCURRED ON THIS SIDE OR THEIRS. ASSISTANCE WAS REQUESTED TO OBTAIN THE PRODUCT AND CLARIFICATION ON WHETHER CONNECTORS AND EDUCATION FOR ENDO WOULD BE REQUIRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24172264 ↗
  • MalfunctionJan 13, 2026Separation Failure

    IT WAS REPORTED THAT THE ENDO HAD EXPERIENCED ISSUES WITH THE 0092110 BLAKEMORE AND STATED THEY HAD BEEN UNABLE TO REMOVE THE PLASTIC PIECES FROM THE END. AT THAT POINT, IT WAS DISCOVERED THAT A POSSIBLE CONNECTOR HAD BEEN MISSING AND THAT EDUCATION WAS NEEDED. SUBSEQUENTLY, A LIST WAS SENT INDICATING THAT THE PRODUCT HAD ACTUALLY BEEN DISCONTINUED, AND THEY HAD PROVIDED THE 0092300 AS THE REPLACEMENT TO ORDER INSTEAD. HOWEVER, IT HAD NOT YET BEEN RECEIVED, AND THE PURCHASE ORDER HAD SOMEHOW BEEN CLOSED. IT WAS UNCLEAR WHETHER THIS OCCURRED ON THIS SIDE OR THEIRS. ASSISTANCE WAS REQUESTED TO OBTAIN THE PRODUCT AND CLARIFICATION ON WHETHER CONNECTORS AND EDUCATION FOR ENDO WOULD BE REQUIRED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24058143 ↗
  • MalfunctionJan 13, 2026Component Missing; Component Misassembled

    IT WAS REPORTED THAT THE ENDO HAD EXPERIENCED ISSUES WITH THE 0092110 BLAKEMORE AND STATED THEY HAD BEEN UNABLE TO REMOVE THE PLASTIC PIECES FROM THE END. AT THAT POINT, IT WAS DISCOVERED THAT A POSSIBLE CONNECTOR HAD BEEN MISSING AND THAT EDUCATION WAS NEEDED. SUBSEQUENTLY, A LIST WAS SENT INDICATING THAT THE PRODUCT HAD ACTUALLY BEEN DISCONTINUED, AND THEY HAD PROVIDED THE 0092300 AS THE REPLACEMENT TO ORDER INSTEAD. HOWEVER, IT HAD NOT YET BEEN RECEIVED, AND THE PURCHASE ORDER HAD SOMEHOW BEEN CLOSED. IT WAS UNCLEAR WHETHER THIS OCCURRED ON THIS SIDE OR THEIRS. ASSISTANCE WAS REQUESTED TO OBTAIN THE PRODUCT AND CLARIFICATION ON WHETHER CONNECTORS AND EDUCATION FOR ENDO WOULD BE REQUIRED. PER THE ADDITIONAL INFORMATION RECEIVED ON 05JAN2026, IT WAS REPORTED THAT THEY NEEDED TO CIRCLE BACK TO THEIR ORIGINAL ISSUE, WHICH WAS ASSISTANCE WITH EDUCATION TO RESOLVE THE PROBLEM OF THE ENDS GETTING STUCK. THEY HAD BEEN TOLD THERE WAS A POTENTIAL ADAPTER THEY MIGHT HAVE BEEN MISSING. THIS WAS ALL BEFORE THEY WERE INFORMED THAT IT WAS NO LONGER BEING MADE, WHICH MADE THEM SWITCH GEARS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24058140 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

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Sources and updates

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