DX-D600 - DXD Imaging Package
Reported: April 12, 2017 Initiated: May 2, 2016 #Z-1738-2017
Product Description
DX-D600 - DXD Imaging Package
Reason for Recall
One of the dent markers from the DX-D600 dropped down from the overhead rail.
Details
- Recalling Firm
- AGFA Healthcare Corp.
- Units Affected
- 81 units
- Distribution
- AL, CA, DC, FL, GA, HI, IL, IN, KS, LA, MA, MN, MO, NV, NJ, NM, NY, OH, OK, OR, SC, TN, TX, VA, and Canada
- Location
- Greenville, SC
Frequently Asked Questions
What product was recalled? ▼
DX-D600 - DXD Imaging Package. Recalled by AGFA Healthcare Corp.. Units affected: 81 units.
Why was this product recalled? ▼
One of the dent markers from the DX-D600 dropped down from the overhead rail.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 12, 2017. Severity: Moderate. Recall number: Z-1738-2017.
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