Luitpold Pharmaceuticals CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4% a) 30 mL SINGLE recall — FDA D-1378-2012
Presence of Particulate Matter: In the course of inspecting retention samples visual particles were observed.
Overview of recall records associated with Luitpold Pharmaceuticals, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Presence of Particulate Matter: In the course of inspecting retention samples visual particles were observed.
This page summarizes recall records in which the official source identifies Luitpold Pharmaceuticals, 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.