AngioSculpt Evo RX PTCA scoring balloon catheter with hydrophilic coating 2200-2015-BRecalls & reported problems
Philips Image Guided Therapy Corporation · 2.0 mm x 15 mm · Class 3
Data updated Oct 18, 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 00813132026813), received between May 31, 2022 and May 31, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Rupture” (1 report).
3 other recalls cover devices cleared under the same FDA submission (P050018); they may or may not involve this specific model.
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
- Material Rupture1
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.
MalfunctionMay 31, 2022Material Rupture; Material Rupture
THE ANGIOSCULPT DEVICE WAS USED TO TREAT A SEVERELY CALCIFIED PROXIMAL LAD. DURING INFLATION AT 6 ATM FOR 5 SECONDS, THE BALLOON RUPTURED. THE PROCEDURE WAS COMPLETED WITH A NEW ANGIOSCULPT DEVICE. NO PATIENT INJURY REPORTED. THIS PRODUCT PROBLEM IS BEING SUBMITTED CONSERVATIVELY BECAUSE THE BALLOON RUPTURED BELOW RBP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14551278 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under P050018. One submission often covers many models, so check the product and lot details in each record.
- Z-0576-2020 · Dec 7, 2018 · TerminatedSpectranetics AngioSculpt PTCA Scoring Balloon Catheter, balloon outer diameter 2.5mm, balloon length 15mm, REF 2027-2515, Sterile, Rx. The firm name on the label is Spectranetics
- Z-2218-2010 · Dec 4, 2009 · TerminatedAngioSculpt Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter, cutting/scoring, Easy Exchange (EX) delivery system, Manufactured by AngioScore, Fremont, CA. Catheter
- Z-0591-2008 · Nov 13, 2007 · TerminatedAngioSculpt PTCA Scoring Balloon Catheter, Catalog (REF) Number: 2027-2510, size 2.5mm x 10 mm, AngioScore, Inc., Fremont, CA.
Other Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring devices
- Wolverine Coronary Cutting Balloon H74939401103000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring1 death36 reports
- Wolverine Coronary Cutting Balloon H74939401103500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring21 reports
- Wolverine Coronary Cutting Balloon H74939401153000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring19 reports
- Wolverine Coronary Cutting Balloon H74939401153500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring19 reports
- Wolverine Coronary Cutting Balloon H74939401104000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring19 reports
- Wolverine Coronary Cutting Balloon H74939401102500Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring16 reports
- Wolverine Coronary Cutting Balloon H74939401154000Boston Scientific Corporation · Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring15 reports
- AngioSculpt PTCA RX Scoring Balloon Catheter 2200-3010Spectranetics Corporation · Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring2 deaths14 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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