TURNPIKE IPN927569Recalls & 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
- 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 10841156110680), received between Apr 30, 2025 and Apr 30, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Material Separation” (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.
Reports received per month
Most reported problems
Device problems
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 30, 2025Material Separation; Material Separation
IT WAS REPORTED THAT: "TIP OF TP LP BROKE OFF IN CALCIFIED LAD.". ADDITIONAL INFORMATION RECEIVED ON 14APR2025: "THE TURNPIKE LP WITH A WIRE STUCK IN THE CATHETER MINUS THE TIP WAS DISCARDED. THE LAD WAS SEVERELY CALCIFIED WITH A MID CTO. THE LPS TIP WAS TRAPPED IN THE LAD CTO. I DIDN'T SEE HOW MANY TIMES THE DOCTOR TORQUED THE CATHETER PER IFU. THE TIP REMAINED IN THE CTO. THE REST OF THE TURNPIKE LP AND WIRE WERE REMOVED OUT OF THE BODY. ONLY A FEW MILLIMETERS OF THE TIP WERE BROKEN OFF IN THE CTO."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21932819 ↗
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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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