Conquest TTC G25472Recalls & reported problems
Cook Incorporated · Conquest TTC Lithotriptor Cable with Adapter · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002254725), received between Jan 13, 2026 and Jan 13, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionJan 13, 2026Break
DURING LITHOTRIPSY, THE PHYSICIAN USED A COOK CONQUEST TTC LITHOTRIPTOR CABLE WITH ADAPTER. IT WAS REPORTED THAT WHEN THE PHYSICIAN INSERTED THIS PRODUCT INTO THE PATIENT, IT COULD NOT BE WITHDRAWN. SIGNIFICANT FORCE WAS ULTIMATELY REQUIRED TO REMOVE IT. SUBSEQUENTLY, THE PRODUCT SHOWED SEVERE VISIBLE TWISTING. THE PROCEDURE WAS COMPLETED WITH A NEW SAME DEVICE. A SECTION OF THE DEVICE DID NOT REMAIN INSIDE THE PATIENT¿S BODY. THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24053777 ↗
Other Lithotriptor, biliary mechanical devices
- Trapezoid RX M00510890Boston Scientific Corporation · Lithotriptor, biliary mechanical482 reports
- Single Use Mechanical Lithotriptor V BML-V442QR-30Olympus Medical Systems Corp. · Lithotriptor, biliary mechanical1 recall1 death269 reports
- Trapezoid RX M00510880Boston Scientific Corporation · Lithotriptor, biliary mechanical1 death287 reports
- Trapezoid RX M00510870Boston Scientific Corporation · Lithotriptor, biliary mechanical149 reports
- Trapezoid RX M00510860Boston Scientific Corporation · Lithotriptor, biliary mechanical1 death53 reports
- Single Use Mechanical Lithotriptor V BML-V437QR-30Olympus Medical Systems Corp. · Lithotriptor, biliary mechanical33 reports
- Single Use Mechanical Lithotriptor V BML-V437QR-30Olympus Medical Systems Corp. · Lithotriptor, Biliary Mechanical21 reports
- Single Use Mechanical Lithotriptor V BML-V242QR-30Olympus Medical Systems Corp. · Lithotriptor, biliary mechanical21 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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