Overview of recall records associated with Arrowhead DE LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.
This page summarizes recall records in which the official source identifies Arrowhead DE 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.
