FDA Device recall Z-1365-2013
MEDITECH Bi-Directional interactive Communication Analyzer Interface
- FDA Device
- Class II
- terminated
- Published 2013-05-29
On 2013-05-29 the FDA classified a Class II recall of MEDITECH Bi-Directional interactive Communication Analyzer Interface by Medical Information Technology, citing incorrect transmission of laboratory results.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1365-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-07 |
| Published | 2013-05-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medical Information Technology |
| Distribution | PR |
Product
MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.
Reason
Incorrect transmission of laboratory results.
Identifiers
| code_info | Magic Releases 5.41, 5.52. 5.53, 5.62, 5.63, 5.64 and Client Server Releases 5.64, 5.65, 6.05, 6.06, 6.07 |
|---|
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-1365-2013%22
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