Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.
FDA Recall #Z-1490-2025 — Class II — February 28, 2025
Product Description
Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.
Reason for Recall
Potential for the gold unlock button to separate from the inserter.
Recalling Firm
Stryker Spine — Allendale, NJ
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
46 units (44 US, 2 OUS)
Distribution
Domestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT. International: Canada.
Code Information
Catalog 48019130; UDI-DI: 07613327501049; Lot Number: 231639;
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated