Stry: Monterey AL Implant Inserter Recall - Gold Button May Separate

Take action

Contact the company & request your remedy

Recalling firmStryker Spine59 State Rt 17 S · Allendale, NJ 07401-1614

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Stryker Spine is recalling Monterey AL Implant Inserter devices (18/20mm, Catalog 48019130) because the gold unlock button might separate. This could cause the device to malfunction during spinal surgery.

Why it’s dangerous

The gold unlock button may detach from the inserter during use, potentially causing the device to malfunction. This could lead to improper spinal implant placement if the button fails to engage correctly.

Who’s affected

Surgical teams using the Monterey AL Implant Inserter for spinal procedures are most at risk. The recall applies to specific model numbers and lot numbers.

How to tell if you have this one

Check for the model number 18/20mm and catalog number 48019130. Affected units also have UDI-DI: 07613327501049 and lot number 231639.

Brand
Stryker Spine
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Identifiers
Look for the model number 18/20mm, catalog number 48019130, UDI-DI: 07613327501049, and lot number 231639.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The gold unlock button may separate from the inserter, potentially causing malfunction during spinal surgery.

How can I tell if my device is affected?

Check for model number 18/20mm, catalog number 48019130, UDI-DI: 07613327501049, and lot number 231639.

What should I do if I have this device?

The recall record does not specify a remedy, so contact Stryker Spine directly for guidance.

Take action

Contact Stryker Spine

We’ve drafted a message you can send Stryker Spine to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1490-2025 — Stryker Spine Stryker Spine

Hello,

I own a Stryker Spine that is covered by recall Z-1490-2025 from Stryker Spine.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1490-2025 (February 28, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1490-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Stryker Spine recalls Monterey AL Implant Inserter; 18/20mm; Catalog 48019130.

Lower-risk recall