Beckman Coulter Inc.

Frequent Recalls

8

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-04-01 to 2026-08-26

Date	Source	Product	Brand	Severity	Units
2026-08-26	FDA Device	FDA Recall: Beckman Coulter DxC 500 AU Clinical Analyzer Modules using software version 1.5 or lower: 1) AU w	Beckman Coulter Inc.	Class II	N/A
2026-08-26	FDA Device	FDA Recall: Beckman Coulter DxC 500i Clinical Analyzer Modules using software version 1.5 or lower: 1) DxC 50	Beckman Coulter Inc.	Class II	N/A
2026-08-12	FDA Device	FDA Recall: REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following in	Beckman Coulter Inc.	Class II	N/A
2026-08-12	FDA Device	FDA Recall: REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following instruments: -	Beckman Coulter Inc.	Class II	N/A
2026-04-29	FDA Device	FDA Recall: Access Total T4 Calibrator, Catalog No. 33805	Beckman Coulter, Inc.	Class II	N/A
2026-04-15	FDA Device	FDA Recall: MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For	Beckman Coulter, Inc.	Class II	N/A
2026-04-15	FDA Device	FDA Recall: MicroScan Neg MIC 3J REF C54814	Beckman Coulter, Inc.	Class II	N/A
2026-04-01	FDA Device	FDA Recall: MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for us	Beckman Coulter, Inc.	Class II	N/A