Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported October 5, 2022
ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-167-01
Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Leading Pharma, LLC recalled ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA… - a low-severity action.
ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA… was recalled by Leading Pharma, LLC in October 5, 2022. Reason: Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules. Check the official notice for the remedy. Verify recall #D-1546-2022 with the FDA Drug before acting.
The recall
Leading Pharma, LLC issued this low-severity FDA Drug recall-Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules.
- Low
- severity level
- Class III
- classification
- October 5, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1546-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1546-2022) was formally reported on October 5, 2022, with the manufacturer initiating the action on August 23, 2022. It is classified under Low severity (Class III), with a current status of Terminated. Leading Pharma, LLC is listed as the recalling firm, operating out of Fairfield, NJ. Federal records list the affected scope as 960 bottles (100 capsules).
The documented reason for this recall is: Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules Distribution data in the federal record shows the product reached: Nationwide within the United States. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
960 bottles (100 capsules)
Related Recalls
6
5 from same agency
Product description
ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-167-01
Reason for recall
Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1546-2022 |
| Date reported | October 5, 2022 |
| Date initiated | August 23, 2022 |
| Recalling firm | Leading Pharma, LLC |
| Firm location | Fairfield, NJ |
| Affected scope | 960 bottles (100 capsules) |
| Distribution | Nationwide within the United States |
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-1546-2022) 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? ▼
ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-167-01. Recalled by Leading Pharma, LLC. Units affected: 960 bottles (100 capsules).
Why was this product recalled? ▼
Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 5, 2022. Severity: Low. Recall number: D-1546-2022.
Where was the recalled product distributed? ▼
Distribution: Nationwide within the United States.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1546-2022) 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.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
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 October 5, 2022. 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.