BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 — Class II medical device recall Z-1701-2017
Terminated recall by Biomet 3i, LLC, reported 2017-04-05. A single lot of product that potentially has a single part within the lot that does not match the product on t
| Recall number | Z-1701-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet 3i, LLC, Palm Beach Gardens, FL, United States |
| Recall initiated | 2017-03-08 |
| Classified | 2017-03-29 |
| Reported by FDA | 2017-04-05 |
| Terminated | 2019-08-02 |
| Countries outside the US | AR |
| Quantity | 5 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00844868009917 |
| Lot numbers | 1199571 |
| Model numbers | LTX610 |
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 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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1701-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.