Soft-Vu 10712006Recalls & reported problems
Angiodynamics, Inc. · Soft-Vu Angiographic Catheter, Sos Omni Selective (2), 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
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI H787107120060), received between Aug 31, 2017 and Aug 9, 2022 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 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
- Detachment of Device or Device Component2
- Difficult to Remove1
- Material Deformation1
- Material Twisted/Bent1
Patient problems
- Device Embedded In Tissue or Plaque2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 9, 2022Difficult to Remove; Material Deformation; Material Twisted/Bent
MID 90¿S MALE WITH HISTORY OF RECENT ACUTE BLOOD LOSS ANEMIA AND GI BLEED. PROCEDURE: ARTERIOGRAM THROUGH RIGHT GROIN. THE ANGIODYNAMICS TWISTED AND KINKED, INSIDE THE PATIENT'S VESSEL. IT WAS VERY DIFFICULT TO REMOVE FROM THE SHEATH. DEVICE WAS REMOVED INTACT, WITHOUT KNOWN HARM TO PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15190438 ↗InjuryAug 14, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED: DR. (B)(6) WAS IN A GI BLEED CASE. DURING THE PROCEDURE, IT WAS NOTED THE SOS 2 CATHETER TIP DISLODGED/DETACHED FROM THE SHAFT OF THE CATHETER IN THE GASTRIC ARTERY. THE DEVICE AND FRAGMENT WERE REMOVED AND THE PROCEDURE WAS COMPLETED WITH A NEW OF THE SAME DEVICE. THEY SAVED THE SOS TIP THAT MALFUNCTIONED TO RETURN TO THE MANUFACTURER FOR EVALUATION. THERE WAS NO PERMANENT HARM OR INJURY TO THE PATIENT, AND THE PATIENT WAS REPORTED AS STABLE POST PROCEDURE. THE REPORTED DEFECTIVE DISPOSABLE DEVICE HAS BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 8893027 ↗InjuryAug 31, 2017Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED TO ANGIODYNAMICS ON AUGUST 14, 2017: IT WAS REPORTED THAT DURING AN ANGIOGRAPHIC PROCEDURE, THE TIP OF THE SOFT-VU SOS 2 DETACHED INSIDE OF THE PATIENT. THE TREATING PHYSICIAN SUCCESSFULLY REMOVED THE FRACTURED TIP VIA SNARE. THE DEVICE WAS SET ASIDE AND A NEW OF THE SAME DEVICE WAS USED TO COMPLETE THE PROCEDURE. THE REPORTED DEFECTIVE DISPOSABLE DEVICE HAS BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 6833577 ↗
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-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-1866-2026 · Mar 3, 2026 · Open, ClassifiedSoft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Quanti
- 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-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-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-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
- 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-1872-2026 · Mar 3, 2026 · Open, ClassifiedAccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box), H
- Z-1869-2026 · Mar 3, 2026 · Open, ClassifiedSoft-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-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-1870-2026 · Mar 3, 2026 · Open, ClassifiedSoft-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-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-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
…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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