FDA recall record

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137 recall — FDA Z-1388-2025

the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high…

Class IIclassification
Z-1388-2025official record ID
Mar 26, 2025report date

Recall record at a glance

Official recordZ-1388-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeckman Coulter, Inc.
Report dateMar 26, 2025
Recall initiation dateFeb 5, 2025
Quantity206 units
LocationChaska, MN, United States

Official product description

DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137.

Why the product was recalled

the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.

Distribution information

US Nationwide. Global Distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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