Nephron Pharmaceuticals Corporation dba Nephron PF-Succinylcholine Chloride Injection, USP recall — FDA D-0154-2020
Incorrect labeling: Incorrect or missing lot and/or exp date
Overview of recall records associated with Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center, including dates, categories and classifications where available.
Classification mix: Class II: 4, Class III: 1.
Incorrect labeling: Incorrect or missing lot and/or exp date
Lack of Assurance of Sterility; bags have potential to leak
GMP Deviations: potential glass contamination
GMP Deviations: potential glass contamination
GMP Deviations: potential glass contamination
This page summarizes recall records in which the official source identifies Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center 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.