Beckman Coulter, Inc.: Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrument

Recall number

Z-3180-2024

Recalling firm

Beckman Coulter, Inc.

Product

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrument

Status

Open, Classified

Initiated

2024-07-10

Posted

2024-09-19

Terminated

not on file

Reason

Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to undersized Pneumatics Tubing in the reagent storage module causing air leaks, compressor failures or sample processing errors. Four complaints were filed for this event that led to Beckman Coulter finding undersized tubing in stock and initiated corrective actions. Use of the affected device may result in errors leading to delay of results.

Root cause

Nonconforming Material/Component

Action

Beckman Coulter issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 7/10/2024 via US mail and email. The notice explained the problem, impact, and requested the following actions be taken: If your laboratory observes either of these system eventscontact the Beckman Coulter Customer Technical Support Center at 1-800-854-3633 (US and Canada) or your local Beckman Coulter representative (outside US and Canada: a). Chassis.Pneumatics MachineControlStatus(Chassis maintain system air pressure failed. 1.The compressor has failed. 2.A large leak exists in the system) b). Pneumatics Air pressure under limit: ### PSI, Chassis.Pneumatics. WS04CompressedAir.32-35psi.PressureSensor. Beckman Coulter will schedule a time to replace the RSM pneumatic tubing.

Quantity

170 units

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, Belgium, Brazil, Croatia, Czech Republic, Egypt, France, Germany, Hungary, Ireland, Israel, Italy, Netherlands, New Zealand, Poland, Portugal, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, United Kingdom.

Lot, serial or model codes

UDI/DI 15099590230623, Serial Numbers: 300116, 300117, 300118, 300123, 300126, 300128, 300129, 300130, 300131, 300133, 300134, 300135, 300136, 300137, 300138, 300139, 300141, 300142, 300143, 300145, 300147, 300148, 300149, 300150, 300151, 300152, 300153, 300154, 300155, 300156, 300157, 300158, 300160, 300161, 300162, 300163, 300164, 300166, 300167, 300168, 300169, 300170, 300171, 300172, 300174, 300176, 300178, 300179, 300180, 300181, 300182, 300183, 300188, 300189, 300190, 300192, 300193, 300194, 300195, 300196, 300197, 300198, 300199, 300200, 300201, 300202, 300203, 300204, 300205, 300206, 300207, 300208, 300209, 300210, 300211, 300212, 300213, 300214, 300215, 300216, 300217, 300218, 300219, 300220, 300221, 300222, 300223, 300224, 300226, 300227, 300228, 300229, 300230, 300231, 300232, 300233, 300234, 300235, 300236, 300237, 300238, 300239, 300240, 300241, 300242, 300243, 300244, 300245, 300246, 300247, 300248, 300249, 300251, 300252, 300253, 300254, 300255, 300256, 300257, 300258, 300260, 300261, 300263, 300264, 300266, 300269, 300270, 300271, 300272, 300273, 300274, 300275, 300276, 300277, 300280, 300281, 300282, 300284, 300285, 300286, 300287, 300291, 300292, 300293, 300294, 300295, 300297, 300307, 300308, 300310, 300312, 300313, 300314, 300315, 300316, 300317, 300319, 300320, 300321, 300322, 300323, 300324, 300325, 300326, 300327, 300328, 300329, 300330, 300332, 300333

510(k) numbers

["K221225"]

PMA numbers

not on file

Product code

JJE

Firm FEI

2122870

Firm city

Chaska

Firm state

MN

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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