ProductGuru Recalls

Official recall record

Beckman Coulter UniCel DxI 600, Part Numbers: A71460, A30260; Photometric Chemistry Analyzer

US FDA — Medical Devices · 2025-10-01 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Recall initiated by firm
2025-10-01
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
15099590369224
Brand on record
Beckman Coulter, Inc.

What the authority reported

An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

Same barcode in other registries

The same EAN appears in 2 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

Other recalls from this brand

All 32 official recall notices naming Beckman Coulter, Inc. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.