FDA Device recall Z-2270-2012
Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
- FDA Device
- Class II
- terminated
- Published 2012-09-05
On 2012-09-05 the FDA classified a Class II recall of Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry by Sunquest Information Systems, citing the recall was initiated because Sunquest has confirmed that the Sunquest Laboratory versions 6.4 and later while using Microbiology Result Entry (MRE), the specimen ribbon contai….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2270-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-12-05 |
| Published | 2012-09-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sunquest Information Systems |
| Distribution | US |
Product
Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
Reason
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory versions 6.4 and later while using Microbiology Result Entry (MRE), the specimen ribbon containing the Accession Number (AN) and the Battery Name may be missing or contain the wrong information.
Identifiers
| code_info | Versions 6.4 and later |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2270-2012%22
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