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Home > Recalled Products > Biologics > Undetermined Hazard > Beckman Coulter Life Sciences FC 500 Series Flow Cytometers (FC 500), COULTER EPICS XL And COULTER EPICS XL-MCL Flow Cytometer With System II Software

Recall: Beckman Coulter Life Sciences FC 500 Series Flow Cytometers (FC 500), COULTER EPICS XL And COULTER EPICS XL-MCL Flow Cytometer With System II Software

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On 2018-11-23, the FDA announced that Beckman Coulter Life Sciences is conducting a recall on FC 500 Series Flow Cytometers (FC 500), COULTER EPICS XL And COULTER EPICS XL-MCL Flow Cytometer With System II Software due to a possible undetermined hazard. The recalled products were sold under the brand name(s) Beckman Coulter Life Sciences during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 1 biologics recalls due to potential undetermined hazard.

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Beckman Coulter Life Sciences, Logo
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Company Contact Information:

Name: Beckman Coulter Life Sciences
Website: www.beckman.com
Phone: 800-369-0333

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Detailed Recall Information



Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.

Product Description: FC 500 Series Flow Cytometers (FC 500), COULTER EPICS XL and COULTER EPICS XL-MCL Flow Cytometer with System II Software

Brand Name(s): Beckman Coulter Life Sciences

Reason for Recall: Undetermined Hazard

Official Recall Date: 2018-11-23


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Additional information provided by the FDA.gov:

Beckman Coulter Life Sciences today announced the previously communicated global voluntary recall launched in January 2018 related to the FC 500 Series Flow Cytometers (FC 500), COULTER EPICS XL and COULTER EPICS XL-MCL Flow Cytometer with System II Software (together referred to as the EPICS) has been classified as Class 1 by the U.S. Food and Drug Administration (FDA). Read More.


More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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