Beckman Coulter AU480 Analyzer Recall

Source: Health Canada · United States

Areazine synthesizes this Health Canada recall directly from Health Canada's official public data feed. See our methodology for full source attribution and refresh cadence.

Beckman Coulter has recalled certain AU480 analyzers due to a software defect that may prevent instrument startup and delay patient test results.

What this Health Canada recall tells you, and what most readers miss

This notice was issued by Health Canada on August 6, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - Product & Food Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.

Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, health-canada, MedicalDevice.

What Happened

Beckman Coulter has determined that a software defect in AU480 chemistry analyzers using Microsoft SQL server 2022 express may cause a DB connection error that renders alarmDB unreadable and prevents instrument startup. The issue is associated with transaction log auto-growth and may cause delays in reporting patient test results to physicians.

Which Products Are Affected

The recall affects the following Beckman Coulter AU Immunochemistry System - AU480 Analyzer units with model AU480 and the following lot or serial numbers: 2021104332, 2021124493, 2022014627, 2021124487, and 2022014611. The company is Beckman Coulter, Inc., 250 S. Kraemer Blvd., Brea, California, United States, 92821.

What You Should Do

No specific consumer action steps are provided in the recall notice.

Why This Matters

The defect may cause delays in reporting patient test results to physicians.

Source

Health Canada

Original source: Health Canada Official Notice ↗

All Product & Food Recalls →

Nationwide notices with similar length or severity timing 8

Two Areazine-derived peer sets for this Health Canada recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.

Frequently Asked Questions

Common questions about this Health Canada recall.

What is this Health Canada recall about?
Beckman Coulter has recalled certain AU480 analyzers due to a software defect that may prevent instrument startup and delay patient test results.
Which agency issued this alert?
This alert was issued by Health Canada. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "medium" severity. Stay informed and follow agency guidance.
What area is affected?
This alert affects United States. Check with Health Canada for the most current geographic scope.
Where can I find more Product & Food Recalls updates?
Browse the full Product & Food Recalls feed on Areazine at areazine.com/ca/recalls/ for the latest updates from Health Canada and other agencies.