---
title: "Monterey AL Implant Inserter; 10/12mm; Catalog 48019100. — FDA record Z-1488-2025 | Is It on Recall"
description: "Potential for the gold unlock button to separate from the inserter."
url: https://isitonrecall.com/recall/fda-device-z-1488-2025-monterey-al-implant-inserter-10-12mm-catalog-48019100/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Monterey AL Implant Inserter; 10/12mm; Catalog 48019100. — FDA record Z-1488-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 28, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.
- **Reason**: Potential for the gold unlock button to separate from the inserter.
- **Classification**: Class II
- **Recalling firm**: Stryker Spine
- **Quantity**: 64 units (60 US, 4 OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1488-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1488-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Catalog 48019100; UDI-DI: 07613327456462; Lot Number: 231634; |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)

## Dates in the source

- **Report date**: Apr 9, 2025
- **Recall initiation date**: Feb 28, 2025
- **Center classification date**: Mar 31, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1488-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Stryker Spine records](https://isitonrecall.com/brand/stryker-spine/)