AGFA Healthcare Corp. recalls AGFA DX-D 100 is a mobile digital radiography x-ray system
- Recall date
- May 29, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1745-2015
- FDA classification
- Class II
- Brand / firm
- AGFA Healthcare Corp.
- Sold / distributed
- US Distribution to the states of : AL, CA, DC, FL, GA, IL, IA, KY, LA, MD, MA, MI, MN, MS, MO, NE, NJ, NY, NC, OH, OK, OR, SC, TN, TX, VA, WV, WI and WY.
Why it was recalled
When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
AGFA DX-D 100 is a mobile digital radiography x-ray system
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