Angiodynamics Worldwide Headquarters: Medical Device Recall in 2012 - (Recall #: Z-2180-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept guidewire: .035 in. --- Catalog No. [REF]: 10734201. Packaged in boxes of 5 catheters each, with manufacturer listed as AngioDynamics, Inc., Queensbury, NY USA. Intended use: angiographic diagnosis.

Product Classification:

Class II

Date Initiated: June 15, 2012

Date Posted: August 15, 2012

Recall Number: Z-2180-2012

Event ID: 62341

Reason for Recall:

AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because one of the catheter pouches within the outer box may be mislabeled.

Status: Terminated

Product Quantity: 7 boxes/35 units

Code Information:

Lot: 564325

Distribution Pattern:

Worldwide distribution: USA (nationwide) including states of: CA, KS, MO, and NC and countries of: Czech Republic and Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated