MicroScan LabPro Data Management System — Class II medical device recall Z-0768-2017
Terminated recall by Beckman Coulter Inc., reported 2016-12-21. Beckman Coulter has received and confirmed reports of an intermittent and unexpected behavior when loading new
| Recall number | Z-0768-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2016-10-25 |
| Classified | 2016-12-15 |
| Reported by FDA | 2016-12-21 |
| Terminated | 2017-05-01 |
| Countries outside the US | MX |
| Model numbers | 6000-0050, 6000-0051, 6000-0052, 6000-0053, 6000-0054, 6000-0060 |
Product
MicroScan LabPro Data Management System. Intended to manage both microbial identification (ID) and antimicrobial agent susceptibility testing (AST) data generated from MicroScan instruments or manually entered microbiology test results, for use by trained laboratory personnel.
Reason for recall
Beckman Coulter has received and confirmed reports of an intermittent and unexpected behavior when loading new panels into a WalkAway instrument using LabPro Data Management System version 4.42. The issue could cause workflow interruption with a potential of delaying reporting results due to the inability to begin processing new panels.
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-0768-2017. 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.