Caterpillar CTP056030URecalls & reported problems
Clearstream Technologies Limited · Caterpillar Arterial Embolization Device, 0.056 Inch ID Catheter Compatibility · Class 2 · Implant
Data updated Oct 16, 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 00801741175565), received between Apr 16, 2021 and Apr 16, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Failure to Advance” (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.
Most reported problems
Device problems
- Failure to Advance1
Patient problems
- Abdominal Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 16, 2021Failure to Advance; Failure to Advance
IT WAS REPORTED THROUGH THE RESULTS OF A CLINICAL TRIAL THAT, DURING PLACEMENT OF AN ARTERIAL EMBOLIZATION DEVICE, THE STUDY DEVICE ALLEGEDLY FAILED TO ADVANCE AND THE DEVICE PLUG DIDN'T GO FORWARD. IT WAS FURTHER REPORTED THAT THE SUBJECT WAS TREATED WITH A NEW DEVICE SUCCESSFULLY. THE PATIENT REPORTEDLY EXPERIENCED ABDOMINAL PAIN, HOWEVER, THE CURRENT STATUS OF PATIENT IS UNKNOWN.
Patient problems: Abdominal Pain
MAUDE report 11676553 ↗
Other Device, Vascular, for Promoting Embolization devices
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- Azur CX Detachable 45-750824Microvention, Inc. · Device, Vascular, for Promoting Embolization115 reports
- Tornado G08261Cook Incorporated · Device, Vascular, for Promoting Embolization2 recalls7 reports
- Optima Coil System OPTI0930CSFMXBalt USA LLC · Device, Vascular, For Promoting Embolization2 recalls4 reports
- Optima Coil System OPTI0720CSFMXBalt USA LLC · Device, Vascular, For Promoting Embolization2 recalls4 reports
- Optima Coil System OPTI0413CSFMXBalt USA LLC · Device, Vascular, For Promoting Embolization2 recalls3 reports
- Prestige Coil System PRES0520HPKPLBalt USA LLC · Device, Vascular, For Promoting Embolization2 recalls3 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 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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