DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137
FDA Device Recall #Z-1326-2025 — Class II — November 13, 2024
Recall Summary
| Recall Number | Z-1326-2025 |
| Classification | Class II — Moderate risk |
| Date Initiated | November 13, 2024 |
| Status | Ongoing |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Beckman Coulter, Inc. |
| Location | Chaska, MN |
| Product Type | Devices |
| Quantity | 245 units |
Product Description
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137
Reason for Recall
The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin freely within the idler pulley housing. When the problem occurs, the analyzer may generate a system event for a Wash Wheel Dispense Arm Spin Mixer Error that is displayed on the navigation bar in the User Interface. The analyzer enters the red system status and will generate a SYS flag. The tests that are in progress may be cancelled and may cause a delay in reporting patient results
Distribution Pattern
US Nationwide. Global Distribution.
Lot / Code Information
UDI-DI: 15099590732103; Serial Numbers: 300116 300117 300123 300124 300126 300128 300129 300130 300131 300132 300133 300134 300135 300136 300137 300138 300139 300141 300142 300143 300144 300145 300147 300148 300149 300150 300151 300152 300153 300154 300155 300156 300157 300158 300161 300162 300163 300164 300166 300167 300168 300169 300170 300171 300172 300173 300174 300176 300177 300178 300179 300181 300182 300183 300186 300188 300189 300190 300191 300192 300193 300194 300195 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 300225 300226 300227 300228 300229 300230 300231 300232 300233 300234 300235 300236 300237 300238 300239 300240 300241 300242 300243 300244 300245 300246 300247 300248 300250 300251 300252 300253 300254 300255 300256 300257 300258 300259 300260 300261 300263 300264 300266 300267 300268 300269 300270 300271 300272 300273 300274 300275 300276 300277 300279 300280 300281 300282 300283 300284 300285 300286 300287 300288 300289 300290 300291 300293 300294 300296 300297 300298 300299 300300 300301 300302 300303 300304 300305 300306 300307 300308 300309 300312 300313 300314 300315 300316 300317 300318 300319 300320 300321 300322 300324 300325 300326 300328 300329 300330 300331 300332 300333 300334 300336 300337 300338 300339 300340 300341 300343 300346 300349 300350 300351 300352 300353 300354 300355 300356 300358 300360 300361 300362 300366 300367 300368 300370 300371 300372 300373 300375 300376 300377 300378 300379 300380 300381 300382 300385 300388 300389 300391 300392 300393 300395 300396 300397 300398 300399 300400 300402 300403 300404 300405 300406 300407 300408
Other Recalls from Beckman Coulter, Inc.
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-1235-2026 | Class II | CellMek SPS Sample Preparation System, REF: C44... | Dec 23, 2025 |
| Z-1025-2026 | Class II | Beckman Coulter UniCel Dxl 600, Part numbers: ... | Nov 26, 2025 |
| Z-1026-2026 | Class II | Beckman Coulter UniCel Dxl 800, Part numbers: ... | Nov 26, 2025 |
| Z-1221-2026 | Class II | COULTER DxH Diluent, REF 628017 COULTER DxH EC... | Nov 10, 2025 |
| Z-0889-2026 | Class II | Access 2 Reaction Vessels, individual, disposab... | Nov 7, 2025 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.