FDA Device recall Z-0046-2018
Power Processor 1K Stockyard
- FDA Device
- Class II
- terminated
- Published 2017-11-01
On 2017-11-01 the FDA classified a Class II recall of Power Processor 1K Stockyard by Beckman Coulter, citing beckman Coulter has identified that due to a PLC software nonconformity the 1K Stockyard can initiate a retrieval of a sample tube during the rack loading process, which should no….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0046-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-08-03 |
| Published | 2017-11-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Beckman Coulter |
| Distribution | n/a |
Product
Power Processor 1K Stockyard. The Power Processor performs all pre-analytical sample tube preparation.
Reason
Beckman Coulter has identified that due to a PLC software nonconformity the 1K Stockyard can initiate a retrieval of a sample tube during the rack loading process, which should not occur. This issue and associated complaint were discovered and filed internally.
Identifiers
| code_info | Software version PLC V26R10 |
|---|
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-0046-2018%22
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