Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:118701

R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD, QTY: (1), STERILE H2O2, REF 71335762. Orthopaedic.

Official recall number

Z-1928-2013

Evidence summary

Product code
MBL
Recall status
Terminated
Event initiated
May 29, 2013
Root cause
Packaging process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1928-2013

Field note

Send feedback

We'll only use this to respond to your feedback.