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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:207612

Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T

Official recall number

Z-2236-2024

Evidence summary

Product code
KWY
Recall status
Open, Classified
Event initiated
April 26, 2024
Root cause
Other
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2236-2024

Field note

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