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Recall Observatory FDA recall evidence

Device product

CERTAIN BELLATEK TITANIUM ABUTMENT 6.0MM Reference Number: IEDAT6

Z-0079-2021

August 31, 2020

Class II

Product summary

Firm
Biomet 3i, LLC
Event
Event 86402
Status
Terminated
Classification
Class II
Quantity
1 unit
Official record key
device-enforcement:Z-0079-2021

Official wording

Reason: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient

Code information: Lot Number: 8562282-1 UDI: (01)00844868031208(10)8562282-1

Distribution pattern: FL, GA, ID, IL, MI, NV, NY, OH, SC, TN, VA

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the definitive abutment will not seat in the correct orientation upon attempted placement with the patient

Field note

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