Drug recall
MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory…
FDA recall event 65158 · Class II · Medical Information Technology, Inc.
Key facts
| Event ID | 65158 |
|---|---|
| Recall numbers | Z-1365-2013 |
| Recalling firm | Medical Information Technology, Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect transmission of laboratory results. |
| Initiation date | May 7, 2013 |
| Report date | May 29, 2013 |
| Termination date | Oct 1, 2014 |
| City | Westwood |
| State | MA |
| Country | United States |
| FEI number | 1000120736 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: