Biomet 3i, LLC: Medical Device Recall in 2017 - (Recall #: Z-1701-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box; one (1) unit per box. Labeled Sterile"

Product Classification:

Class II

Date Initiated: March 8, 2017

Date Posted: April 5, 2017

Recall Number: Z-1701-2017

Event ID: 76809

Reason for Recall:

A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier

Status: Terminated

Product Quantity: 5

Code Information:

LTX610, lot 1199571; UDI: (01)00844868009917(17)210916(10)1199571

Distribution Pattern:

Argentina

Voluntary or Mandated:

Voluntary: Firm initiated