Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Reported: July 26, 2017 Initiated: December 21, 2016 #Z-2735-2017
Product Description
Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Reason for Recall
A customer reported that when using an NX workstation with software version NX 3.0.8950 software and selecting the affected patient/exam from closed exams, initially the wrong image was linked to the exam and appeared. After a short time the wrong image was replaced by the correct image, however the wrong image was used for transmitting to PACS.
Details
- Recalling Firm
- AGFA Healthcare Corp.
- Units Affected
- 221 units
- Distribution
- AL, AZ, AR, CA, DC, FL, GA, IL, IN, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NJ, NY, NC, OH, OK, PA, SC, SD, TN, TX, UT, VA, WA, WV and Canada
- Location
- Greenville, SC
Frequently Asked Questions
What product was recalled? ▼
Agfa Healthcare NX 3.0.8950 Imaging Processing Software. Recalled by AGFA Healthcare Corp.. Units affected: 221 units.
Why was this product recalled? ▼
A customer reported that when using an NX workstation with software version NX 3.0.8950 software and selecting the affected patient/exam from closed exams, initially the wrong image was linked to the exam and appeared. After a short time the wrong image was replaced by the correct image, however the wrong image was used for transmitting to PACS.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 26, 2017. Severity: Moderate. Recall number: Z-2735-2017.
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