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PILLING IPN005374Recalls & reported problems

Teleflex Incorporated · DEBAKEY HEPARIN NEEDLE SMALL · Class 1

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 24026704517200), received between Mar 24, 2023 and Mar 24, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Dull, Blunt” (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

  • Dull, Blunt1

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.

  • MalfunctionMar 24, 2023Dull, Blunt; Dull, Blunt

    REPORTED ISSUE: THE DEVICE SNAPPED/BROKE IN TWO PIECES WHERE THE NEEDLE AND HUB CONNECT, DURING USE. THE PATIENT WAS UNDERGOING AN EXTENDED HYSTERECTOMY. NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16615117 ↗

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Sources and updates

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