Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size), Powder for oral suspension, Rx only, Manufactured for: L
Summary
The FDA issued a Class II for Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size), Powder for oral by Lupin Pharmaceuticals Inc.. Reason: Failed Content Uniformity Specifications.
Details
Source
Drug Recall
External ID
D-0559-2024
Action Date
2024-06-26
Status
Terminated
Category
drug
Product Description
Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size), Powder for oral suspension, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore Maryland, Manufactured by: Lupin Limited, Mandideep, India NDC 68180-407-03
Lot/Code Info: Lot F201519, Expiry: November 2024
Quantity Affected: 3,552 bottles
Reason for Recall
Failed Content Uniformity Specifications
Distribution
Nationwide in the US
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-30
Company
Baltimore, MD
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 33 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Lupin Pharmaceuticals Inc. has 49 FDA actions in our database, including 49 recalls.
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 (Lupin Pharmaceuticals Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lupin Pharmaceuticals Inc. have FDA actions?
Lupin Pharmaceuticals Inc. has 49 FDA actions in our database, including 49 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0559-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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