Mckesson Information Solutions LLC: Medical Device Recall in 2014 - (Recall #: Z-0042-2015)

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:

McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.

Product Classification:

Class II

Date Initiated: August 27, 2014

Date Posted: October 15, 2014

Recall Number: Z-0042-2015

Event ID: 69377

Reason for Recall:

Software Error: The McKesson Cardiology Hemo calculation section incorrectly converts the Hemoglobin value before it is utilized in the applicable formula calculations.

Status: Terminated

Product Quantity: 272 devices

Code Information:

McKesson CardiologyTM Hemo versions: 13.0, 13.0HF1, 13.0HF2, 13.0HF3, 13.1.

Distribution Pattern:

Worldwide distribution: US (nationwide) including states of: AR, CA, FL, DE, GA, HI, IL, IN, KS, LA, MA, MD, MN, MO, MS, MT, NJ, NV, OK, PA, SC, TNTX, , UT, WA; and countries of: Australia, Canada, Israel and the United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated