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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:124899

CPT 12/14 COCR (various sizes)

Official recall number

Z-1032-2014

Evidence summary

Product code
JDI
Recall status
Terminated
Event initiated
October 11, 2013
Root cause
Packaging
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1032-2014

Field note

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