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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:143777

TF Adaptive Gutta Percha Point Size SM3 50pk, Part No. 815-1541 Intended to fill a endontontically obturated root canal treatment

Official recall number

Z-1083-2016

Evidence summary

Product code
EKM
Recall status
Terminated
Event initiated
February 08, 2016
Root cause
Error in labeling
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1083-2016

Field note

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