Class II
Medical Device Recall: 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 PO
SPINEART SA · June 30, 2025
Reason for Recall
Cannulated fenestrated polyaxial screws may be incorrectly labeled
Product Description
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
Distribution
US Nationwide distribution in the states of Florida , Kentucky, California.
States Affected
NATIONWIDE
Quantity Affected
0
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2280-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.