Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count
Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a bottle of Methylergonovine Maleate tablets
Every FDA drug recall initiated in 2019, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.
1,788 recalls, newest first.
Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a bottle of Methylergonovine Maleate tablets
Lack of Assurance of Sterility: Bags have potential to leak.
CGMPs Deviations: Insufficient Quality Assurance controls over critical systems in the manufacturing facility.
Failed Dissolution Specifications
Presence of Foreign Substance; Product complaints received related to brownish/blackish stains on the tablets and brownish/blackish powder observed inside the bottles.
Subpotent Drug
Subpotent Drug
Failed Content Uniformity Specifications: Out-of-specification result observed in uniformity of containers test at 9 month long term stability condition for upright orientation.
Microbial Contamination of Non-Sterile Products: Out-of-specification results for Microbial Enumeration Tests USP <61> was observed.
CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.
CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.
CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.
CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.
CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.
CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Marketed without an Approved NDA/ANDA: The product may be construed a sunscreen due to labeling of the product and comments about the product found on e-commerce websites.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.