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Soft-Vu 10714033Recalls & reported problems

Angiodynamics, Inc. · Soft-Vu Angiographic Catheter, Hockey Stick (1), Non-Braided · 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 H787107140330), received between Dec 15, 2016 and Dec 15, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Device Issue” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Issue1
  • Material Perforation1
  • Material Puncture/Hole1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • InjuryDec 15, 2016Material Puncture/Hole; Material Perforation; Device Issue; Material Puncture/Hole; Material Perforation; Device Issue

    AS REPORTED DECEMBER 07, 2016, A (B)(6), FEMALE PATIENT PRESENTED FOR AN MEDICAL PROCEDURE. DURING THE PROCEDURE, STANDARD ATRAUMATIC STEEL WIRE WAS USED WITH THE HOCKEY STICK FOR ACCESS IN A BILIARY DRAINAGE CASE. AS THE GUIDE WIRE WAS THREADED USING NORMAL, ATRAUMATIC PROCEDURE, INSTEAD OF STRAIGHTENING THE CATHETER TIP, THE GUIDE WIRE PERFORATED THE CATHETER SIDE WALL. NO ADVERSE OUTCOME FOR PATIENT, PROCEDURE CARRIED ON TO CONCLUSION. THE GUIDE WIRE PRODUCT USED - COOK ROSEN CURVED GUIDE WIRE - STANDARD FOR THE PROCEDURE. CATHETER REMOVED INTACT. THERE WAS NO HARM OR INJURY TO THE PATIENT DUE TO THIS EVENT. THE REPORTED DEFECTIVE DISPOSABLE DEVICE IS AVAILABLE FOR RETURN TO THE MANUFACTURER FOR EVALUATION.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 6178520 ↗

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-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-1875-2026 · Mar 3, 2026 · Open, Classified
    AccuVu 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-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-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-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-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),
  • 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-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-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-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-1861-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-1858-2026 · Mar 3, 2026 · Open, Classified
    Soft-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-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

…and 8 more.

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Sources and updates

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