Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

3I OSSEOTITE CERTAIN DENTAL IMPLANTS Recalled by Biomet 3i, LLC Due to Product was incorrectly packaged.

Date: August 8, 2016
Company: Biomet 3i, LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Biomet 3i, LLC directly.

Affected Products

3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.

Quantity: 92 units

Why Was This Recalled?

Product was incorrectly packaged.

Where Was This Sold?

This product was distributed to 2 states: CA, FL

Affected (2 states)Not affected

About Biomet 3i, LLC

Biomet 3i, LLC has 222 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report