Spineart Sa recalls

All Spineart Sa recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (2).

2 recalls published between August 20, 2025 and August 20, 2025.

• PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model recall
  FDA August 20, 2025 · Spineart Sa · Class II
• PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model recall
  FDA August 20, 2025 · Spineart Sa · Class II