Diamondback Peripheral DBP-175SOLID180 (REF 7-10029-03)Recalls & reported problems
Cardiovascular Systems, Inc. · Diamondback Peripheral, Radial Access OAD, 1.75mm, 30mm, 180cm shaft · Class 2
Data updated Oct 13, 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 10852528005374), received between Mar 16, 2020 and Mar 16, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Entrapment of Device” (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.
Most reported problems
Device problems
- Entrapment of Device1
Patient problems
- Vessel Or Plaque, Device Embedded In1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 16, 2020Entrapment of Device; Entrapment of Device
THE EXTENDED LENGTH DIAMONDBACK PERIPHERAL ORBITAL ATHERECTOMY DEVICE WAS USED TO TREAT A 95% STENOSED, HEAVILY CALCIFIED LESION IN THE DISTAL SUPERFICIAL FEMORAL ARTERY. FOLLOWING ONE TREATMENT PASS, THE DEVICE STALLED AND BECAME STUCK IN THE VESSEL. SURGERY WAS PERFORMED TO REMOVE THE DEVICE, AND THE PATIENT WAS IN STABLE CONDITION FOLLOWING THE PROCEDURE. THE PATIENT WAS DISCHARGED (B)(6) 2020.
Patient problems: Vessel Or Plaque, Device Embedded In
MAUDE report 9836177 ↗
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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 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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