SPINEART SA: Medical Device Recalls in 2025

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by SPINEART SA in 2025. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 55 45-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW
Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW Component: No