Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:206546

Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular applications such as in the venous, arterial, biliary and renal system REFERENCE PART NUMBER (RPN): DTN-18-20.0 ORDER NUMBER (GPN): G01377

Official recall number

Z-1526-2024

Evidence summary

Product code
DRC
Recall status
Open, Classified
Event initiated
March 01, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1526-2024

Field note

Send feedback

We'll only use this to respond to your feedback.