Beckman Coulter Inc Customized Automation Centrifuge, First and Second Generation. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Customized Automation Centrifuge, First and Second Generation.
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
First Generation: OPIC0004, HAND0007, HAND0008, HAND0011, HAND0012, U9507151, U9507152, U9507153. Second Generation: 2028, 2030, 2032, 2033, 2034, 2038, 2039, 2040.
Products Sold
First Generation: OPIC0004, HAND0007, HAND0008, HAND0011, HAND0012, U9507151, U9507152, U9507153. Second Generation: 2028, 2030, 2032, 2033, 2034, 2038, 2039, 2040.
Beckman Coulter Inc is recalling Customized Automation Centrifuge, First and Second Generation. due to Centrifuge loss of containment with potential for injury or exposure to biohazard among lab workers.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Centrifuge loss of containment with potential for injury or exposure to biohazard among lab workers.
Recommended Action
Per FDA guidance
Recall was by letter and by telephone. All customers have been contacted.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026