AGFA Healthcare Corp. recalls DX-D600 - DXD Imaging Package
- Recall date
- May 2, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1738-2017
- FDA classification
- Class II
- Brand / firm
- AGFA Healthcare Corp.
- Sold / distributed
- 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
Why it was recalled
One of the dent markers from the DX-D600 dropped down from the overhead rail.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DX-D600 - DXD Imaging Package
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