Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman Coulter is recalling the AQUIOS CL System...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Beckman Coulter Inc. directly.
Affected Products
AQUIOS CL Flow Cytometer, Catalog No. B30166; Intended for use with in vitro diagnostic flow cytometry applications using up to four florescent detection channels.
Quantity: 148 units total (12 units in US)
Why Was This Recalled?
Beckman Coulter is recalling the AQUIOS CL System because the use of the reagent carousel can lead to misalignment of the carousel and damage to the prep probe.
Where Was This Sold?
This product was distributed to 7 states: FL, GA, IL, NY, PA, SC, WA
About Beckman Coulter Inc.
Beckman Coulter Inc. has 241 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report