FDA recall record

Leadiant Biosciences Abelcet recall — FDA D-0327-2023

Lack of assurance of sterility: Medial fill with presence of Cupriavidus pauculus.

Class IIclassification
D-0327-2023official record ID
Feb 22, 2023report date

Recall record at a glance

Official recordD-0327-2023
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLeadiant Biosciences, Inc.
Report dateFeb 22, 2023
Recall initiation dateFeb 3, 2023
Quantity31,879 vials
LocationGaithersburg, MD, United States

Official product description

Abelcet (Amphotericin B Lipid Complex) Injection, 5 mg/mL, 100 mg vial, Rx only, Manufactured by Exelead, Inc., Indianapolis, IN 46268; Distributed by Leadiant Biosciences, Inc., Gaithersburg, MD 20878, NDC 57665-101-41

Why the product was recalled

Lack of assurance of sterility: Medial fill with presence of Cupriavidus pauculus.

Distribution information

Nationwide USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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