Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury,
Summary
The FDA issued a Class II for Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Ph by SUN PHARMACEUTICAL INDUSTRIES INC. Reason: Subpotent drug.
Details
Source
Drug Recall
External ID
D-0891-2023
Action Date
2023-07-05
Status
Terminated
Category
drug
Product Description
Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by Sun Pharmaceutical Medicare Limited, Baska Ujeti Road, Ujeti, Halol-389350, Gujarat, India, NDC 62756-0233-01
Lot/Code Info: Lot # BAD0089A, Exp 01/2025; BAD0330A, Exp 07/2025
Quantity Affected: 12960 vials
Reason for Recall
Subpotent drug
Distribution
USA nationwide
Type: N/A
Recall Initiated: 2023-05-30
Company
Princeton, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 40 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
SUN PHARMACEUTICAL INDUSTRIES INC has 84 FDA actions in our database, including 83 recalls and 1 clearance.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SUN PHARMACEUTICAL INDUSTRIES INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SUN PHARMACEUTICAL INDUSTRIES INC have FDA actions?
SUN PHARMACEUTICAL INDUSTRIES INC has 84 FDA actions in our database, including 83 recalls and 1 device clearance.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0891-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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