Spineart Sa Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland
This page shows every FDA and USDA recall linked to Spineart Sa Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
6
Total Recalls
2019
First Recall
2025
Most Recent
Brand Name: PERLA TL MIS
Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW
Model/Catalog Number: MPF-PS 65...
Aug 8, 2025
· Device
Open, Classified
Brand Name: PERLA TL MIS
Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW
Model/Catalog Number: MPF-PS 55...
Aug 8, 2025
· Device
Open, Classified
PERLA TL 25D SCREW REF:
TLF-DS 45 25-S
TLF-DS 45 30-S
TLF-DS 45 35-S
TLF-DS 45 40-S
TLF-DS 45 45-S
TLF-DS 55...
May 3, 2024
· Device
Open, Classified
JULIET Ti LL, LATERAL LUMBAR TI-LIFE PLATE SMALL, REF: JLT-PL 02 08-S, JLT-PL 02 10-S, JLT-PL 02 12-S, JLT-PL...
Apr 24, 2023
· Device
Open, Classified
PERLA TL Lateral Connector Open - Product Usage: intended to be used with autograft and/or allograft. Pediatri...
Apr 9, 2021
· Device
Terminated
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Nov 22, 2019
· Device
Terminated