Osseotite and Nanotite Implants (2013-08-26) — recall 50138
Health Canada — Medical Devices · Canada · 2013-11-07 · Type III
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Archived by the issuing authority — kept for reference
Reported risk: A visually observable condition which may be present on some of the implants have been identified. The condition is caused by the implant coming into contact with residual machining fluid which may have been left on the packaging insert. The condition does not meet the cleanliness criteria of Biomet 3i.
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