A L I Technologies Ltd: Medical Device Recall in 2025 - (Recall #: Z-0958-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Change Healthcare Cardiology Hemo software

Product Classification:

Class II

Date Initiated: December 2, 2024

Date Posted: January 22, 2025

Recall Number: Z-0958-2025

Event ID: 96025

Reason for Recall:

Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).

Status: Ongoing

Product Quantity: 204 units

Code Information:

Software version/UDI: 14.1.1/(01)17540262100020, 14.2/(01)17540262100037, 14.3/(01)17540262100044, 14.3.2/(01)17540262100051, 15.01/(01)17540262100105, 15.1/(01)17540262100129

Distribution Pattern:

US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, PA, SC, SD, TN, TX, WA, WI and the countries of Australia, Israel, Canada, Germany, Ireland, United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated