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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:145895

Slip-Cath Beacon Tip Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques.

Official recall number

Z-2614-2016

Evidence summary

Product code
DQO
Recall status
Terminated
Event initiated
April 15, 2016
Root cause
Unknown/Undetermined by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2614-2016

Field note

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