Exact FDA event identifier

Event 96025

3 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: December 02, 2024
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: A L I Technologies Ltd

Dossier provenance

Source snapshots represented here

openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

McKesson Cardiology Hemo software

Z-0957-2025

Recall number: Z-0957-2025
Initiated: December 02, 2024
Classification: Class II
Status: Ongoing
Recalling firm: A L I Technologies Ltd
Quantity: 1 unit

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0

Software defect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Software versions: 13.1.2/No UDI, 13.2.1/UDI:(01)80010939050010, 14/(01)80010939050027,

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.

device · product 2 of 3

Change Healthcare Cardiology Hemo software

Z-0958-2025

Recall number: Z-0958-2025
Initiated: December 02, 2024
Classification: Class II
Status: Ongoing
Recalling firm: A L I Technologies Ltd
Quantity: 204 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0

Software defect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

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

device · product 3 of 3

Change Healthcare Cardiology Hemodynamics software

Z-0959-2025

Recall number: Z-0959-2025
Initiated: December 02, 2024
Classification: Class II
Status: Ongoing
Recalling firm: A L I Technologies Ltd
Quantity: 2 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0

Software defect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Software version 15.01/UDI:(01)17540262100129