Medical DeviceSep 14, 2016
Biomet Microfixation Hard Tissue Replacement (HTR) Implant, Rx only, for use in single recall — FDA Z-2751-2016
Potential sterility deficiency.
Class IIFDA: TerminatedBiomet Microfixation, LLC
Recall history in this database
Classification mix: Class II: 3.
Medical DeviceOct 28, 2015
Biomet Microfixation Neuro Combo Set Case The cases hold surgical instrumentation in place recall — FDA Z-0136-2016
The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force.
Class IIFDA: TerminatedBiomet Microfixation, LLC
Medical DeviceOct 28, 2015
Biomet Microfixation Thinflap System Case The cases hold surgical instrumentation in place recall — FDA Z-0137-2016
The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force.
Class IIFDA: TerminatedBiomet Microfixation, LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies Biomet Microfixation, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.