Severity
Moderate
ModerateClass IIOngoing
FDA Drug recall · Reported November 20, 2024
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98
Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Cipla USA, Inc. recalled Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for … - a moderate-severity action.
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for … was recalled by Cipla USA, Inc. in November 20, 2024. Reason: Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.. Check the official notice for the remedy. Verify recall #D-0043-2025 with the FDA Drug before acting.
The recall
Cipla USA, Inc. issued this moderate-severity FDA Drug recall-Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets..
- Moderate
- severity level
- Class II
- classification
- November 20, 2024
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0043-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0043-2025) was formally reported on November 20, 2024, with the manufacturer initiating the action on October 23, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Cipla USA, Inc. is listed as the recalling firm, operating out of Warren, NJ. Federal records list the affected scope as 1,875 boxes (cipla and exlan).
The documented reason for this recall is: Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets. Distribution data in the federal record shows the product reached: USA nationwide.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
1,875 boxes (cipla and exlan)
Related Recalls
6
5 from same agency
Product description
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98
Reason for recall
Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0043-2025 |
| Date reported | November 20, 2024 |
| Date initiated | October 23, 2024 |
| Recalling firm | Cipla USA, Inc. |
| Firm location | Warren, NJ |
| Affected scope | 1,875 boxes (cipla and exlan) |
| Distribution | USA nationwide. |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0043-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Cipla USA, NDC 69097-0936-98. Recalled by Cipla USA, Inc.. Units affected: 1,875 boxes (cipla and exlan).
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 20, 2024. Severity: Moderate. Recall number: D-0043-2025.
Where was the recalled product distributed? ▼
Distribution: USA nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0043-2025) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported November 20, 2024. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.