Medical Information Technology, Inc.
Medical Information Technology, Inc. has 4 FDA enforcement events on this register (4 product records) between 2013 and 2025: 4 device; the busiest year was 2014 with 2.
0% of its events are Class I; the most common class is Class II (4). 1 event is listed as ongoing; the recalling firm's address is in MA.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 5 Feb 2025 | MEDITECH Expanse Laboratory (LAB), Microbiology (MIC), Anatomical Pathology (PTH), Genetics (GEN). Calculator/data processing module for clinical use. | Device | Class II | 1 | Ongoing |
| 21 Feb 2014 | MEDITECH Microbiology; Client Server Releases 5.6, 5.65, 5.66, 5.67, 6.0, 6.05, 6.07, 6.1, 6.13 and 6.14. Integrates requisition, specimen processing, and patient information with data in the healthcare information system (HCIS). | Device | Class II | 1 | Terminated |
| 17 Jan 2014 | MEDITECH Microbiology - Calculator/data processing module, for clinical use. | Device | Class II | 1 | Terminated |
| 7 May 2013 | 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. | Device | Class II | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Medical Information Technology, Inc. had?
4 enforcement events (4 product records) on this register, 2013–2025: 4 device.
Are any Medical Information Technology, Inc. recalls ongoing?
1 event is listed as ongoing in the current openFDA export.
What class are Medical Information Technology, Inc. recalls?
4 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.