Merge LIS
Reported: November 4, 2020 Initiated: January 23, 2017 #Z-0289-2021
Product Description
Merge LIS
Reason for Recall
A defect in the software resulted in medications that are not associated with the patient (i.e., medications that the patient is not currently taking) appearing on their report.
Details
- Recalling Firm
- Merge Healthcare, Inc.
- Units Affected
- 47 units
- Distribution
- Domestic Distribution Only: Alabama, California, Colorado, Connecticut, Florida, Georgia, Illinois, Kentucky, Louisiana, Maryland, Michigan, Mississippi, Oklahoma, Tennessee, Texas.
- Location
- Hartland, WI
Frequently Asked Questions
What product was recalled? ▼
Merge LIS. Recalled by Merge Healthcare, Inc.. Units affected: 47 units.
Why was this product recalled? ▼
A defect in the software resulted in medications that are not associated with the patient (i.e., medications that the patient is not currently taking) appearing on their report.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 4, 2020. Severity: Moderate. Recall number: Z-0289-2021.
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