Overview of recall records associated with Advanced Accelerator Applications USA, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 2, Class II: 1.
Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Subpotent Drug: low out-of-specification results for Vial 1 assay obtained during stability studies.
Defective Container: loose aluminum cap crimp for the dilution buffer vial present in the NETSPOT Kit (vial 2).
This page summarizes recall records in which the official source identifies Advanced Accelerator Applications USA, Inc. 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.
