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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:155960

Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USTMCA85200

Official recall number

Z-2529-2017

Evidence summary

Product code
DYB
Recall status
Terminated
Event initiated
May 22, 2017
Root cause
Packaging
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2529-2017

Field note

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