Class II — Medical Information Technology, Inc.
| Recalling firm | MEDICAL INFORMATION TECHNOLOGY, INC. |
|---|---|
| Registered facility | Medical Information Technology, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Incorrect transmission of laboratory results. |
| 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. |
| Quantity | 56 devices |
| Distribution | Worldwide Distribution - USA, including Puerto Rico and the country of Canada. |
| Initiated | 2013-05-07 |
| Classified | 2013-05-22 |
| Terminated | 2014-10-01 |
| Recall number | Z-1365-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medical Information Technology, Inc. (Z-1365-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65158/
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