PILLING IPN005930Recalls & reported problems
Teleflex Incorporated · Class 1
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 24026704522112), received between Apr 1, 2021 and Aug 1, 2022 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (5 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break5
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
BROKEN, DEFECTIVE JAW OR TIP PART.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15138193 ↗MalfunctionApr 13, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11655268 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11602172 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11602168 ↗
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- PILLING IPN005932Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR18 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.