TURNPIKE IPN039140Recalls & reported problems
Teleflex Incorporated · Turnpike LP, 135cm · Class 2
All models of TURNPIKE (18)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10841156105044), received between Apr 12, 2021 and Feb 18, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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 18, 2026.
Most reported problems
Device problems
- Fracture1
- Separation Problem1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 18, 2022Fracture; Fracture
AS REPORTED: TIP FRACTURE. DOCTOR WAS ABLE TO TRAP AND REMOVE THE BROKEN PIECE OF THE TIP FROM THE LAD.
Patient problems: Foreign Body In Patient
MAUDE report 13564130 ↗MalfunctionApr 12, 2021Separation Problem; Separation Problem
AS REPORTED: DURING USE ON A PATIENT, THE TIP SEPARATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11648085 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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