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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:114390

Trilogy F/M Acetabular Shell without holes. Several ODs: 40MM, 42MM, 44MM, 46MM, 48MM, 50MM, 52MM, 54MM, 56MM, 58MM, 60MM, 62MM, 64MM, 66MM, 68MM, 70MM. The Trilogy Acetabular System is indicated for either cemented or uncemented use in individuals undergoing surgery for rehabilitating hip damage.

Official recall number

Z-0769-2013

Evidence summary

Product code
LPH
Recall status
Terminated
Event initiated
September 14, 2012
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0769-2013

Field note

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