Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen P
Summary
The FDA issued a Class II for Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack car by Cipla USA, Inc.. Reason: Failed stability specifications: Out of specification for hardness test.
Details
Source
Drug Recall
External ID
D-0217-2026
Action Date
2025-12-17
Status
Ongoing
Category
drug
Product Description
Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., Hauppauge, NY 11786, Manufactured for : Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-936-98.
Lot/Code Info: lot# NB240315, exp 12/31/2025
Quantity Affected: 1180 boxes
Reason for Recall
Failed stability specifications: Out of specification for hardness test
Distribution
Nationwide in the USA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-24
Company
Warren, 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 54 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Cipla USA, Inc. has 20 FDA actions in our database, including 20 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 (Cipla USA, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cipla USA, Inc. have FDA actions?
Cipla USA, Inc. has 20 FDA actions in our database, including 20 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0217-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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