McKesson Israel Ltd.: Medical Device Recall in 2015 - (Recall #: Z-0910-2015)

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:

McKesson Cardiology ECG Management It is a software application designed to import, display, store, analyze, distribute and manage information related to ECG procedures of adult and pediatric patients from external ECG devices.

Product Classification:

Class II

Date Initiated: December 19, 2014

Date Posted: January 14, 2015

Recall Number: Z-0910-2015

Event ID: 70144

Reason for Recall:

An ECG procedure time stamp is incorrect, due to a software error in the McKesson Cardiology ECG Management with software versions 13.1 and 13.1.1.

Status: Terminated

Product Quantity: 9

Code Information:

MC13.1 and MC13.1.1

Distribution Pattern:

Worldwide Distribution - USA including MA, MS, NH, NC, TX, WA and Internationally to the United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated