Medical DeviceSep 4, 2024
Agfa N.V DR 800. Digital Radiography X-ray System recall — FDA Z-2738-2024
Potential for the front lever chain of the DR 800 table to fail.
Class IIFDA: OngoingAgfa N.V.
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceApr 10, 2024
Agfa DX-D 100 system-Digital Radiography mobile X-ray System recall — FDA Z-1462-2024
Steel cable installed inside the mobile column which supports the weight of the telescopic arm with the tube head has potential risk -an interference could cause the safety system which…
Class IIFDA: OngoingAgfa N.V.
Understanding this recall history
This page summarizes recall records in which the official source identifies Agfa N.V. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.