Device evidence

device-recall:cfres:170155

Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).

Official recall number

Z-0852-2019

Evidence summary

Product code: DQX
Recall status: Terminated
Event initiated: December 19, 2018
Root cause: Labeling mix-ups
Source snapshot: d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product: Z-0852-2019