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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:144306

Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in total knee arthroplasty. REF 42-5114-008-18

Official recall number

Z-1341-2016

Evidence summary

Product code
JWH
Recall status
Terminated
Event initiated
March 17, 2016
Root cause
Employee error
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1341-2016

Field note

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