AAP Implantate Ag recall — FDA Z-1675-2020
The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris…
Overview of recall records associated with AAP Implantate Ag, including dates, categories and classifications where available.
Classification mix: Class II: 2.
The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris…
There is the potential for the Lambotte chisel to break at the welded piece parts of the chisel body and knocking plate.
This page summarizes recall records in which the official source identifies AAP Implantate Ag 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.