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PILLING IPN029212Recalls & reported problems

Teleflex Incorporated · MALONEY TUNGSTEN FILLED BOUGIE 32 FRENCH · Class 2

All models of PILLING (28)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704642202), received between Jul 11, 2023 and Jul 11, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Delivered as Unsterile Product” (1 report).

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 16, 2026.

Most reported problems

Device problems

  • Delivered as Unsterile Product1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 11, 2023Delivered as Unsterile Product; Delivered as Unsterile Product

    IT WAS REPORTED THAT PRIOR TO USE IT WAS FOUND THAT "SPOTS" WERE FOUND ALL OVER THE DEVICE. NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17298767 ↗

Other Bougie, esophageal, and gastrointestinal, gastro-urology devices

All Bougie, esophageal, and gastrointestinal, gastro-urology devices →

Sources and updates

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