Soft-Vu 10709402Recalls & reported problems
Angiodynamics, Inc. · Soft-Vu Angiographic Catheter, Renal, Braided · Class 2
All models of Soft-Vu (54)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI H787107094020), received between May 10, 2017 and May 10, 2017 — classified as 3 injuries.
The most frequently reported specific device problem is “Difficult to Advance” (3 reports).
23 other recalls cover devices cleared under the same FDA submission (K112452, K161596, K173762); 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 16, 2026.
Most reported problems
Device problems
- Difficult to Advance3
- Entrapment of Device3
Patient problems
- Aortic Dissection3
- Patient Problem/Medical Problem3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMay 10, 2017Entrapment of Device; Difficult to Advance; Entrapment of Device; Difficult to Advance
AS REPORTED TO ANGIODYNAMICS ON APRIL 10, 2017: THE TREATING PHYSICIAN REPORTED THAT DURING THE ANGIOGRAPHIC PROCEDURE, THE ANGIOGRAPHIC CATHETER SEEMED DIFFICULT TO MANIPULATE. WHILE ADVANCING THE CATHETER, THE TIP OF THE CATHETER CAUSED DISSECTION OF THE ARTERY WALL. IT WAS REPORTED THE DEFECTIVE DISPOSABLE DEVICE IS AVAILABLE FOR RETURN TO THE MANUFACTURER FOR EVALUATION.
Patient problems: Aortic Dissection; Patient Problem/Medical Problem
MAUDE report 6556398 ↗InjuryMay 10, 2017Entrapment of Device; Difficult to Advance; Entrapment of Device; Difficult to Advance
AS REPORTED TO ANGIODYNAMICS ON APRIL 10, 2017: THE TREATING PHYSICIAN REPORTED THAT DURING THE ANGIOGRAPHIC PROCEDURE, THE ANGIOGRAPHIC CATHETER SEEMED DIFFICULT TO MANIPULATE. WHILE ADVANCING THE CATHETER, THE TIP OF THE CATHETER CAUSED DISSECTION OF THE ARTERY WALL. IT WAS REPORTED THE DEFECTIVE DISPOSABLE DEVICE IS AVAILABLE FOR RETURN TO THE MANUFACTURER FOR EVALUATION.
Patient problems: Aortic Dissection; Patient Problem/Medical Problem
MAUDE report 6556397 ↗InjuryMay 10, 2017Entrapment of Device; Difficult to Advance; Entrapment of Device; Difficult to Advance
AS REPORTED TO ANGIODYNAMICS ON APRIL 10, 2017: THE TREATING PHYSICIAN REPORTED THAT DURING THE ANGIOGRAPHIC PROCEDURE, THE ANGIOGRAPHIC CATHETER SEEMED DIFFICULT TO MANIPULATE. WHILE ADVANCING THE CATHETER, THE TIP OF THE CATHETER CAUSED DISSECTION OF THE ARTERY WALL. IT WAS REPORTED THE DEFECTIVE DISPOSABLE DEVICE IS AVAILABLE FOR RETURN TO THE MANUFACTURER FOR EVALUATION.
Patient problems: Aortic Dissection; Patient Problem/Medical Problem
MAUDE report 6556396 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K112452, K161596, K173762. One submission often covers many models, so check the product and lot details in each record.
- Z-1860-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog No.: 10714009; Product/UPN No.: H787107140095 (Box), H787107140090 (Pouch); Box Qu
- Z-1875-2026 · Mar 3, 2026 · Open, ClassifiedAccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM; Catalog No.: 13709804; Product/UPN No.: H787137098045 (Box), H
- Z-1857-2026 · Mar 3, 2026 · Open, ClassifiedSoft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013; Product/UPN No.: H787107100135 (Box), H787107100130 (Pouch); Box Quanti
- Z-1863-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Product/UPN No.: H787107140165 (Box), H787107140160 (Pouch); Box Q
- Z-1856-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103; Product/UPN No.: H787107071035 (Box), H787107071030 (Pouch); Box Quan
- Z-1858-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001; Product/UPN No.: H787107140015 (Box), H787107140010 (Pouch); Box Qua
- Z-1867-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0SH; Catalog No.: 10714024; Product/UPN No.: H787107140245 (Box), H787107140240 (Po
- Z-1861-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011; Product/UPN No.: H787107140115 (Box), H787107140110 (Pouch); Box Qua
- Z-1864-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Product/UPN No.: H787107140175 (Box), H787107140170 (Pouch); Box Qu
- Z-1865-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018; Product/UPN No.: H787107140185 (Box), H787107140180 (Pouch); Box Qu
- Z-1868-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040; Product/UPN No.: H787107140405 (Box), H787107140400 (Pouch); B
- Z-1859-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.: 10714002; Product/UPN No.: H787107140025 (Box), H787107140020 (Pouch); Box Quant
- Z-1874-2026 · Mar 3, 2026 · Open, ClassifiedAccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Box),
- Z-1873-2026 · Mar 3, 2026 · Open, ClassifiedAccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Catalog No.: 13709604; Product/UPN No.: H78
- Z-1862-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (Box), H787107140140 (Pouch); Box Quantit
…and 8 more.
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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