Recall Z-3180-2024 ยท JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
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
| Date | Sep 19, 2024 (initiated Jul 10, 2024) |
| Status | Open, Classified |
| 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). Pneumati |
| 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 K |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K221225 | Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer Beckman Coulter, Inc., Nov 10, 2022 |