Angiodynamics, Inc.: Medical Device Recall in 2014 - (Recall #: Z-2261-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 30 cm Infusion Pattern, Catalog No./REF 12401808, Product No. H787124018085, STERILE -- AngioDynamics, 603 Queensbury Avenue, Queensbury, NY 12804

Product Classification:

Class II

Date Initiated: August 6, 2014

Date Posted: August 27, 2014

Recall Number: Z-2261-2014

Event ID: 68980

Reason for Recall:

AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).

Status: Terminated

Product Quantity: Domestic: 81 units; Foreign: 13 units

Code Information:

Lot 4731641 (exp. date 31-Mar-17)

Distribution Pattern:

Worldwide Distribution - USA (nationwide) and Internationally to Austria, Australia, Ireland, Malaysia, Sweden, and Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated