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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:178501

Drill Tapered WP 5x11.5 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.

Official recall number

Z-1312-2020

Evidence summary

Product code
DZI
Recall status
Terminated
Event initiated
March 14, 2019
Root cause
Packaging process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1312-2020

Field note

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