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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:143501

Stryker, T2 Guidewire, Ball-Tipped, 2.5 x 1000mm Product Usage: Intended for the temporary stabilization of bone segments or fragments.

Official recall number

Z-0877-2016

Evidence summary

Product code
MAY
Recall status
Terminated
Event initiated
January 21, 2016
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0877-2016

Field note

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