FDA recall record

BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within recall — FDA Z-1701-2017

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…

Class IIclassification
Z-1701-2017official record ID
Apr 5, 2017report date

Recall record at a glance

Official recordZ-1701-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBiomet 3i, LLC
Report dateApr 5, 2017
Recall initiation dateMar 8, 2017
Quantity5
LocationPalm Beach Gardens, FL, United States

Official 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"

Why the product was recalled

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

Distribution information

Argentina

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.