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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:117230

CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.

Official recall number

Z-1095-2013

Evidence summary

Product code
EAP
Recall status
Terminated
Event initiated
September 18, 2012
Root cause
Radiation Control for Health and Safety Act
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1095-2013

Field note

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