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Recall Observatory FDA recall evidence

Device product

Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens, FL 33410 USA 1-800-342-5454***EDAZ , EDAZx and ILDExxx***BellaTek Zirconia Abutment Position Number: XX Abutment; Pilier; Abutment; Abutment; Pilastro; Pilar***Rx only***Non-sterile, Sterilize prior to use.***Biomet 3i Dental Iberica S.L.*** Biomet 3i Dental Abutments are intended for use as accessories to endosseous dental implants to support prostheses in edentulous or partially edentulous patients. These are intended for use to support single and multiple tooth prostheses.

Z-1215-2014

August 26, 2013

Class II

Product summary

Firm
Biomet 3i, LLC
Event
Event 66787
Status
Terminated
Classification
Class II
Quantity
10,454
Official record key
device-enforcement:Z-1215-2014

Official wording

Reason: Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures were received.

Code information: All lots of products made since April 1, 2011. Catalog model EDAZ, EDAZx and ILDExxx

Distribution pattern: Worldwide Distribution: US (nationwide) including states of: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, KS, KY, LA, MA, MD, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, Hawaii and Puerto Rico; and countries of: Spain, Australia, Canada, Colombia, Japan, Uruguay, Mexico, Estonia, United Kingdom, Denmark, Germany, Spain, Italy, Poland, Ireland Netherlands, France, Sweden, Portugal, Australia, France, Belgium, Switzerland, Norway, Czech Republic, France, Holland, and Luxembourg.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures were received.