Central Admixture Pharmacy Services Total Parental Nutrition - Pediatric PN Patient-Specific recall — FDA D-0740-2026
Incorrect Product Formulation
Browse U.S. drug recall enforcement reports from the FDA in a structured, searchable format. Review the recalled product, reason, firm, status, dates, distribution information and FDA classification when available.
754 detailed records are currently available in this category.
Incorrect Product Formulation
CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.
Presence of precipitate
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month stability
Lack of Assurance of Sterility
Subpotent Drug
Lack of Assurance of Sterility
Subpotent Drug
Presence of Particulate Matter: Hair was found in products
Subpotent Drug
Lack of Assurance of Sterility
Presence of Particulate Matter: Hair was found in products
Lack of Assurance of Sterility
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testing for 12…
Presence of Particulate Matter: Hair was found in products
Lack of Assurance of Sterility
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
Subpotent Drug
Lack of Assurance of Sterility
A drug recall record can include the reason for recall, firm, status, distribution pattern, quantity and FDA classification. This site does not provide medical advice; it organizes public recall information and links users back to official sources.
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