PILLING IPN005932Recalls & reported problems
Teleflex Incorporated · Class 1
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 24026704522129), received between Apr 1, 2021 and Aug 3, 2022 — classified as 18 malfunctions.
The most frequently reported specific device problem is “Break” (18 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
- Break18
Patient problems
- No Clinical Signs, Symptoms or Conditions18
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 3, 2022Break; Break
USED IN A CARDIAC CASE JAW BROKE OFF NO HARM TO THE PATIENT, THEY USED ANOTHER ONE THAT WAS ON HAND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15159391 ↗MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
MalfunctionAug 1, 2022Break; Break
BROKEN, DEFECTIVE JAW OR TIP PART.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15138266 ↗MalfunctionApr 13, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11655194 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11603420 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11603415 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11603396 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11603385 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11603362 ↗MalfunctionApr 1, 2021Break; Break
BROKEN JAW, TIP NOT ALIGNED AND NOT BITING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11602187 ↗
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- Lead Clippers G20003Cook Vandergrift Inc. · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- ADVANTA SLIDER GDS 22125Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- Needle NDL-107-04Galt Medical Corp. · Instruments, Surgical, Cardiovascular1 recall0 reports
- ADVANTA SLIDER GDS 22092Atrium Medical Corporation · INSTRUMENTS, SURGICAL, CARDIOVASCULAR1 recall0 reports
- PILLING IPN915270Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR16 reports
- PILLING IPN915271Teleflex Incorporated · INSTRUMENTS, SURGICAL, CARDIOVASCULAR5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.