Overview of recall records associated with Biomet 3i, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 108, Class III: 1.
During recent revised sterilization validation testing, the included surgical trays did not meet the Sterility Assurance Level required.
During recent revised sterilization validation testing, the included surgical trays did not meet the Sterility Assurance Level required.
During recent revised sterilization validation testing, the included surgical trays did not meet the Sterility Assurance Level required.
During recent revised sterilization validation testing, the included surgical trays did not meet the Sterility Assurance Level required.
During recent revised sterilization validation testing, the included surgical trays did not meet the Sterility Assurance Level required.
One of the dental implants do not have the internal hex feature. One of the dental implants do not have the internal thread feature.
One of the dental implants do not have the internal hex feature. One of the dental implants do not have the internal thread feature.
A small number of outer implant boxes may be mislabeled. The inner tray, containing the implant, is label correctly. This condition, if present and not recognized could potentially result…
A small number of outer implant boxes may be mislabeled. The inner tray, containing the implant, is label correctly. This condition, if present and not recognized could potentially result…
Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full OSSEOTITE Parallel Walled Certain Implant due to a manufacturing condition where the depth of the implant's internal hex…
Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full OSSEOTITE Parallel Walled Certain Implant due to a manufacturing condition where the depth of the implant's internal hex…
Biomet 3i recalled their Osseotite Tapered Certain Implant, Model # INT510 due to a small percentage of the devices are missing the internal threading.
Biomet 3i conducted a recall on the device Low Profile Abutment, Non-Hexed Castable Cylinder due to some packages labeled LPCCC1, Hexed Castable Cylinder possibly containing LPCCC2,…
This page summarizes recall records in which the official source identifies Biomet 3i, 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.
