Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.

FDA Recall #Z-1488-2025 — Class II — February 28, 2025

Recall #Z-1488-2025 Date: February 28, 2025 Classification: Class II Status: Ongoing

Product Description

Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.

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

64 units (60 US, 4 OUS)

Distribution

Domestic: CA, CO, FL, GA, IL, MA, NE, NH, NY, OK, PA, TX, UT. International: Canada.

Code Information

Catalog 48019100; UDI-DI: 07613327456462; Lot Number: 231634;

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated