Merge LIS software.
Reported: November 23, 2016 Initiated: March 5, 2015 #Z-0399-2017
Product Description
Merge LIS software.
Reason for Recall
There is a potential for duplicate container numbers to be created for patients.
Details
- Recalling Firm
- Merge Healthcare, Inc.
- Units Affected
- 413 sites potentially have the affected software
- Distribution
- Distribution was made nationwide and to the Virgin Islands. Foreign distribution was made to the Bahamas.
- Location
- Hartland, WI
Frequently Asked Questions
What product was recalled? ▼
Merge LIS software.. Recalled by Merge Healthcare, Inc.. Units affected: 413 sites potentially have the affected software.
Why was this product recalled? ▼
There is a potential for duplicate container numbers to be created for patients.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 23, 2016. Severity: Moderate. Recall number: Z-0399-2017.
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