Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:209189

Stryker iBur 4.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and Endoscopic applications Ref: 8431-013-040DC

Official recall number

Z-2728-2024

Evidence summary

Product code
HBE
Recall status
Completed
Event initiated
July 24, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2728-2024

Field note

Send feedback

We'll only use this to respond to your feedback.