FDA Device recall Z-2900-2016
AQUIOS CL Flow Cytometer, Catalog No. B30166
- FDA Device
- Class II
- terminated
- Published 2016-10-05
On 2016-10-05 the FDA classified a Class II recall of AQUIOS CL Flow Cytometer, Catalog No. B30166 by Beckman Coulter, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2900-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-09-06 |
| Published | 2016-10-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Beckman Coulter |
| Distribution | FL, GA, IL, NY, PA, SC, WA |
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
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.
Identifiers
| code_info | AY20032 AZ19046 AZ12030 AY51072 AZ19047 AZ15044 AY47071 AZ15038 AY47063 AZ12033 AZ19052 AY51075 AY03004 AZ12027 AY25038 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2900-2016%22
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