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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:140969

Stryker Radius 5.5 to 3.5 Rod to Red Connector, REF 48664530. Intended to provide additional support during fusion using autograft or allograft in skeletally mature patients.

Official recall number

Z-0270-2016

Evidence summary

Product code
NKB
Recall status
Terminated
Event initiated
September 25, 2015
Root cause
No Marketing Application
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0270-2016

Field note

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