AQUIOS CL Flow Cytometer — Class II medical device recall Z-2900-2016
Terminated recall by Beckman Coulter Inc., reported 2016-10-05, distributed in FL, GA, IL, NY, PA, SC, WA. Beckman Coulter is recalling the AQUIOS CL System because the use of the reagent carousel can lead to misalign
| Recall number | Z-2900-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2016-09-06 |
| Classified | 2016-09-28 |
| Reported by FDA | 2016-10-05 |
| Terminated | 2017-08-07 |
| Distributed | FL, GA, IL, NY, PA, SC, WA |
| Countries outside the US | AU, BE, CA, CH, CL, CZ, DE, DK, ES, FI, FR, GB, GH, IL, IT, MY, NL, PA, PL, RO, SE, SK, ZA |
| Model numbers | B30166 |
Product
AQUIOS CL Flow Cytometer, Catalog No. B30166; Intended for use with in vitro diagnostic flow cytometry applications using up to four florescent detection channels.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2900-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.