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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:144236

Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, 9784130131 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

Official recall number

Z-1064-2017

Evidence summary

Product code
KXJ
Recall status
Open, Classified
Event initiated
February 19, 2016
Root cause
Device Design
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-1064-2017

Field note

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