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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:155139

Willscher Vas Skewers, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.

Official recall number

Z-2311-2017

Evidence summary

Product code
KOA
Recall status
Terminated
Event initiated
May 01, 2017
Root cause
Under Investigation by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2311-2017

Field note

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