FDA recall record

Biomet 3i Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product Usage recall — FDA Z-2208-2013

One of the dental implants do not have the internal hex feature. One of the dental implants do not have the internal thread feature.

Class IIclassification
Z-2208-2013official record ID
Sep 25, 2013report date

Recall record at a glance

Official recordZ-2208-2013
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBiomet 3i, LLC
Report dateSep 25, 2013
Recall initiation dateJun 10, 2013
Quantity178
LocationPalm Beach Gardens, FL, United States

Official product description

Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product Usage: Surgical placement in the upper or lower jaw to provide a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple single teeth utilizing delayed or immediate loading or with a terminal or intermediary abutment for fixed or removable bridgework and to retain over dentures.

Why the product was recalled

One of the dental implants do not have the internal hex feature. One of the dental implants do not have the internal thread feature.

Distribution information

Worldwide Distribution - USA Nationwide in the states of MA, CT, NJ, DE, NY, FL, OK, TX, PA, DC, IL, KS, LA, MD, CA, RI, TN, MN, and SC and the countries of Canada, Japan, Australia, Italy Germany, France, Switzerland, Apain, Brazil, Uruguay, Singapore, Dominican Republic, Taiwan, Austria, Portugal, and the United Kingdom.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.