A L I Technologies recalls

A L I Technologies has 3 recalls on record with the FDA and USDA, the earliest in 2025 and the latest reported on 22 Jan 2025. 3 are still ongoing. The most frequent reason is device malfunction.

Total recalls3since 2025

Last 12 months0reported

Class I00% of total

Ongoing3latest 22 Jan 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 3Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why a l i technologies is recalled

Device Malfunction3100%

Product types

Medical Software3100%

By year

20253100%

Ongoing a l i technologies recalls

3 active

Reported	Class	Recall	Company	Reason	Where
22 Jan 2025Device	CLASS II	Change Healthcare Cardiology Hemodynamics recalled by A L I Technologies	A L I Technologies	Device Malfunction	Nationwide
22 Jan 2025Device	CLASS II	McKesson Cardiology Hemo recalled by A L I Technologies	A L I Technologies	Device Malfunction	Nationwide
22 Jan 2025Device	CLASS II	Change Healthcare Cardiology Hemo recalled by A L I Technologies	A L I Technologies	Device Malfunction	Nationwide

All a l i technologies recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
22 Jan 2025Device	CLASS II	Change Healthcare Cardiology Hemodynamics recalled by A L I Technologies	A L I Technologies	Device Malfunction	Nationwide
22 Jan 2025Device	CLASS II	McKesson Cardiology Hemo recalled by A L I Technologies	A L I Technologies	Device Malfunction	Nationwide
22 Jan 2025Device	CLASS II	Change Healthcare Cardiology Hemo recalled by A L I Technologies	A L I Technologies	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.