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Soft-Vu 50702301Recalls & reported problems

Angiodynamics, Inc. · Soft-Vu Angiographic Catheter, Berenstein, Non-Braided · Class 2

All models of Soft-Vu (54)

Data updated Oct 16, 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 H787507023010), received between Aug 3, 2020 and Aug 3, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

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

  • Fracture1

Patient problems

  • Device Embedded In Tissue or Plaque1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 3, 2020Fracture; Fracture

    AN ANGIODYNAMICS TERRITORY MANAGER REPORTED AN ISSUE WITH A 4 FR. BERNSTEIN CATHETER. DURING A PROCEDURE, THE PHYSICIAN WAS TRYING TO ADVANCE THE CATHETER, WITHOUT RESISTANCE, AND NOTED THAT THE TIP WAS NOT VISIBLE. THE PHYSICIAN ATTEMPTED TO REMOVE THE CATHETER BUT HAD DIFFICULTY. ONCE REMOVED, IT WAS NOTICED THAT APPROXIMATELY 6" FROM THE TIP, WAS A LARGE FRACTURE. IT WAS ALMOST COMPLETELY BROKEN AND WAS CLOSE TO BREAKING OFF INSIDE OF THE PATIENT. ULTIMATELY, THE PROCEDURE WAS COMPLETED WITH ANOTHER SAME DEVICE AND THERE WAS NO PATIENT HARM OR ADVERSE EVENT REPORTED BY THE END USER. THE REPORTED DEVICE HAS BEEN RETURNED TO THE MANUFACTURER AND AN INVESTIGATION INTO THE ROOT CAUSE FOR EVENT IS CURRENTLY IN PROGRESS.

    Patient problems: Device Embedded In Tissue or Plaque

    MAUDE report 10359623 ↗

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-1856-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1859-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1867-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1870-2026 · Mar 3, 2026 · Open, Classified
    Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog No.: 10732301; Product/UPN No.: H787107323015 (Box), H787107323010 (Pouch); Box Qua
  • Z-1862-2026 · Mar 3, 2026 · Open, Classified
    Soft-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
  • Z-1863-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1865-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1869-2026 · Mar 3, 2026 · Open, Classified
    Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Catalog No.: 10731401; Product/UPN No.: H787107314015 (Box), H787107314010 (Pouch);
  • Z-1873-2026 · Mar 3, 2026 · Open, Classified
    AccuVu 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-1857-2026 · Mar 3, 2026 · Open, Classified
    Soft -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-1868-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1871-2026 · Mar 3, 2026 · Open, Classified
    Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN No.: H787107343015 (Box), H787107343010 (Pouch); Box Quantit
  • Z-1860-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1864-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1874-2026 · Mar 3, 2026 · Open, Classified
    AccuVu 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),

…and 8 more.

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Sources and updates

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