Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1861-2026Class II

Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No...

Boston Scientific Corporation / initiated 2026-03-03 / Open, Classified / root cause: manufacturing process

Angiodynamics, Inc. began a recall of 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)... on . FDA classified it as Class II and gives the reason as "The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub". As of , the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1861-2026
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
Boston Scientific Corporation
Product
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 Quantity: 5 pouches;
Product code
DQO Catheter, Intravascular, Diagnostic
Reason for recall
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
On March 3, 2026 URGENT VOLUNTARY MEDICAL DEVICE RECALL letters were sent to customers. Actions to be taken: IMMEDIATELY: 1. Stop using the devices subject to this recall and share the notification to all users of the deviceswithin your facility immediately. 2. Provide a copy of this recall notification to all sites or clinics to which you have distributed affectedproduct. 3. Remove any affected items/lots from your inventory (whether in labs, Central Supply, Shipping andReceiving or ANY other location). 4. Segregate this product in a secure location for return to AngioDynamics, Inc. 5. Package and Return the Recalled Product.
Quantity in commerce
435 units (87 boxes)
Distribution
Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon, Netherlands, New Zealand, Panama, Slovenia, South Africa, Spain, Sweden, Thailand.
Product codes and lots
SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011; Product/UPN No.: H787107140115 (Box), H787107140110 (Pouch); UDI-DI: 25051684007877(Box), 15051684007870(Pouch); Lot No.: A3025038, A3025051;

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1861-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1856-2026Class IIOngoingVoluntary: Firm initiated
Z-1857-2026Class IIOngoingVoluntary: Firm initiated
Z-1858-2026Class IIOngoingVoluntary: Firm initiated
Z-1859-2026Class IIOngoingVoluntary: Firm initiated
Z-1860-2026Class IIOngoingVoluntary: Firm initiated
Z-1861-2026Class IIOngoingVoluntary: Firm initiated
Z-1862-2026Class IIOngoingVoluntary: Firm initiated
Z-1863-2026Class IIOngoingVoluntary: Firm initiated
Z-1864-2026Class IIOngoingVoluntary: Firm initiated
Z-1865-2026Class IIOngoingVoluntary: Firm initiated
Z-1866-2026Class IIOngoingVoluntary: Firm initiated
Z-1867-2026Class IIOngoingVoluntary: Firm initiated
Z-1868-2026Class IIOngoingVoluntary: Firm initiated
Z-1869-2026Class IIOngoingVoluntary: Firm initiated
Z-1870-2026Class IIOngoingVoluntary: Firm initiated
Z-1871-2026Class IIOngoingVoluntary: Firm initiated
Z-1872-2026Class IIOngoingVoluntary: Firm initiated
Z-1873-2026Class IIOngoingVoluntary: Firm initiated
Z-1874-2026Class IIOngoingVoluntary: Firm initiated
Z-1875-2026Class IIOngoingVoluntary: Firm initiated