Reported Apr 12, 2017 · Terminated
DX-D600 - DXD Imaging Package
AGFA Healthcare Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: AGFA Healthcare Corp. · 10 S Academy St · Greenville, SC · 29601-2632
Is this the product you have?
- DX-D600 - DXD Imaging Package
- Lot codes and dates
88 of 88 codes
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
- Amount recalled
- 81 units
Where it was sold
Why it was recalled
One of the dent markers from the DX-D600 dropped down from the overhead rail.
This product could cause temporary or reversible health problems — stop using it.
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