Forza Ti Spacer System Recall: Labeling Claims Not Consistently Present

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Contact the company & request your remedy

Recalling firmOrthofix U.S. LLC3451 Plano Pkwy, N/A · Lewisville, TX 75056-9453

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Orthofix U.S. LLC is recalling Forza Ti Spacer Systems with specific model numbers (38-2006SP to 38-3914SP) because their labeling claims are not consistently present. This issue does not pose a safety hazard but requires attention to ensure accurate product information.

Why it’s dangerous

The recall is due to labeling claims that are not consistently present across the product line. This means the product information may vary, but it does not involve a safety hazard or risk of injury.

Who’s affected

Users of Forza Ti Spacer Systems with model numbers 38-2006SP through 38-3914SP are affected. Individuals who have these specific models are most at risk due to inconsistent labeling.

How to tell if you have this one

Check for model numbers starting with 38-2006SP through 38-3914SP on the product packaging or label. The product is sold as Forza Ti Spacer Systems with specific dimensions and lengths.

Brand
Forza Ti
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for model numbers starting with 38-2006SP through 38-3914SP on the product packaging or label.

✎ GovInfoNow

Questions people ask

Is this product dangerous?

No, this recall is for inconsistent labeling claims, not a safety hazard. The product does not pose a risk of injury or damage.

What should I do if I have this product?

The recall does not specify a remedy. Check the product label for the model number to see if it falls within the recalled range.

How can I confirm if my product is recalled?

Look for model numbers starting with 38-2006SP through 38-3914SP on the product packaging or label.

Take action

Contact Forza Ti

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

✉️ Open in email

Subject: Recall Z-0895-2026 — Forza Ti Forza Ti

Hello,

I own a Forza Ti that is covered by recall Z-0895-2026 from Forza Ti.

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.

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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-0895-2026 (November 3, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0895-2026 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.

Orthofix U.S. LLC recalls Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti

Lower-risk recall