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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:187367

Atec Insignia Anterior Cervical Plate System, REF 136-0119, Insignia, ACP, 1-Level, 19 mm, Rx Only, Non-Sterile, UDI: (01)00190376268453

Official recall number

Z-1802-2021

Evidence summary

Product code
KWQ
Recall status
Terminated
Event initiated
April 26, 2021
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1802-2021