Angiodynamics: Medical Device Recall in 2015 - (Recall #: Z-1143-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No. 700-103909; 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615; and 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615

Product Classification:

Class II

Date Initiated: December 19, 2014

Date Posted: March 4, 2015

Recall Number: Z-1143-2015

Event ID: 70388

Reason for Recall:

Printed mark on the trocar intended to indicate a 5cm distance from the distal tip of the needle is actually located 4cm from the distal tip of the needle.

Status: Terminated

Product Quantity: 43

Code Information:

Lot No. 4773676, 4776428 and 4780110

Distribution Pattern:

Worldwide Distribution - US Distribution to the states of AZ, AR, FL, MI, MN, MO, NY, TX, VA, WA and WI., and to the countries of Hungary and Spain.

Voluntary or Mandated:

Voluntary: Firm initiated