FDA Device recall Z-1701-2017
BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box
- FDA Device
- Class II
- terminated
- Published 2017-04-05
On 2017-04-05 the FDA classified a Class II recall of BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box by Biomet 3i, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1701-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-08 |
| Published | 2017-04-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Biomet 3i |
| Distribution | n/a |
Product
BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box; one (1) unit per box. Labeled Sterile"
Reason
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
Identifiers
| code_info | LTX610, lot 1199571; UDI: (01)00844868009917(17)210916(10)1199571 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1701-2017%22
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