Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:210101

Soltive Premium SuperPulsed Laser - Intended for incision, excision, resection, ablation, coagulation, hemostasis, and vaporization of soft tissue, Model/Catalog Number: TFL-PLS

Official recall number

Z-0134-2025

Evidence summary

Product code
GEX
Recall status
Open, Classified
Event initiated
August 13, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0134-2025

Field note

Send feedback

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