Reported Sep 4, 2024 · Ongoing
DR 800. Digital Radiography X-ray System.
Agfa N.V.
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 N.V. · Septestraat 27 · Mortsel · N/A
Is this the product you have?
- DR 800. Digital Radiography X-ray System.
- Lot codes and dates
- Type No. 6010/200
- UDI-DI
280 of 280 codes
05414904251805Device Serial No. 9259459489499901003102211161136116112291239140114041453146014891506153215681704173317571888189319501954195720102070213022442297237123782901293130683217150764376390391593096998499210321042104910521123114811971217132313411203
- Amount recalled
- 141 units
Where it was sold
Why it was recalled
Potential for the front lever chain of the DR 800 table to fail.
This product could cause temporary or reversible health problems — stop using it.
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