TURNPIKE IPN039143Recalls & reported problems
Teleflex Incorporated · Turnpike Spiral, 150cm · Class 2
All models of TURNPIKE (18)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841156105099), received between May 6, 2021 and May 6, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED: WHILE USING THE TURNPIKE SPIRAL CATHETER TO ATTEMPT TO CROSS A MODERATELY TORTUOUS AND HEAVILY CALCIFIED LAD LESION, THE CATHETER BECAME BROKEN, LEAVING 1/3 OF THE CATHETER IN THE PATIENT'S VESSEL. MULTIPLE ATTEMPTS TO RETRIEVE THE SECTION WERE UNSUCCESSFULLY MADE. PATIENT IS STABLE, NO COMPLAINTS OVERNIGHT, RESTED COMFORTABLY. RECEIVED MW5100722 ON (B)(6) 2021. REPORTED: WHILE USING THE TURNPIKE SPIRAL CATHETER TO ATTEMPT TO CROSS AN LAD LESION, TIP BROKE OFF IN PATIENT'S DIAGONAL ARTERY GRAFT; 1/3 OF THE CATHETER IN THE PATIENT'S VESSEL. MULTIPLE ATTEMPTS TO RETRIEVE THE SECTION WERE UNSUCCESSFULLY MADE. ADDITIONAL INFORMATION RECEIVED FROM FACILITY ON (B)(6) 2021: REPORTED: ESTIMATED THAT 2CM OF THE DISTAL TIP REMAINED ATTACHED TO THE CATHETER AND WAS REMOVED. REMAINING PIECE WAS UNABLE TO BE RETRIEVED WITH A SNARE, LEFT IN THE VESSEL, NOT STENTED TO THE WALL.
Patient problems: Foreign Body In Patient
MAUDE report 11785317 ↗
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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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