Every recall we track for Agfa N.V. — 7 in all — plus the complaints and injury reports the public filed about them.
Agfa recalls DR 800 digital radiography x-ray systems with potential front lever chain failure. Affected units have specific serial numbers; stop using immediately to prevent injury.
Agfa recalls DX-D 100 mobile X-ray systems with potential cable interference causing safety system failure and patient injury. Models 5411/050, A5411/0300, A5411/0400 affected.
Agfa recalls DR 800 X-Ray systems with MUSICA Dynamic (Type 6010/200) due to potential incorrect dose calculations during fluoroscopy exams. Affected units have specific serial numbers; users should contact Agfa for details.
Agfa recalls DR 800 X-ray systems with TomoSynthesis that may not stop image acquisition after expected exposures, posing a risk of overexposure. Affected units have specific serial numbers.
Agfa recalls DR 800 X-Ray systems with model numbers 00925, 00945, 00949, 1136 due to possible fluoroscopy area mismatch with detector, risking inaccurate imaging.
Agfa recalls PET plates coated film with pinholes visible in dark images. Affected models include XJUB8, XJM73, XJUDD, XJM85, EKLYZ. No remedy specified in recall notice.
Agfa recalls specific DX-D 600 ceiling-mounted X-ray systems due to potential cable failure that could cause equipment to fall, harming patients or others. Affected units have serial numbers starting with A5430000015.
