TURNPIKE IPN927570Recalls & reported problems
Teleflex Incorporated · Turnpike LP, 150cm · Class 2
All models of TURNPIKE (18)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10841156110697), received between Jul 25, 2024 and Dec 4, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Difficult to Remove” (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.
Reports received per month
Most reported problems
Device problems
- Difficult to Remove1
- Material Separation1
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.
InjuryDec 4, 2024Difficult to Remove; Material Separation; Difficult to Remove; Material Separation
IT WAS REPORTED THAT: "MICROCATHETER WAS ADVANCED THROUGH CX THEN THROUGH EPICARDIAL FOR RETROGRADE PROCEDURE IN CTO. AFTER ENCOUNTERING SOME RESISTANCE AND MICROCATHETER SHOWING SOME SIGNS OF FATIGUE, OPERATOR ATTEMPTED TO REMOVE THE DEVICE. EVEN WITH PULL BACK AND TORQUING, DEVICE WAS NOT REMOVABLE. OPERATOR USED ROTABURR TO CUT THE DEVICE. NEEDS TO KNOW IF DEVICE IS MRI COMPATIBLE AS THEY WOULD LIKE TO RUN AN MRI ON THE PATIENT."
Patient problems: Foreign Body In Patient
MAUDE report 20840668 ↗InjuryJul 25, 2024
TUENPIKE LP CATHETER LOT # 73B24001018, REF 5639, EXP 2026-02-27. CAME APART WHILE IN USE AND ADHERED TO GUIDE WIRE. BOTH PIECES WERE RETRIEVED BY PERFORMING PHYSICIAN. NO IMPACT TO PATIENT OR OTHERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19839562 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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