Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported July 21, 2021
NIFEdipine EXTENDED-RELEASE TABLETS, USP 30 mg Rx only packaged as a) 100 count unit dose carton, NDC 0904-7080-61; b) 50 count unit dose carton, NDC 0904-7080-06: Distributed by: Ingenus Pharmaceuticals, LLC Orlando, FL 32839-6408 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA
Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
The Harvard Drug Group recalled NIFEdipine EXTENDED-RELEASE TABLETS, USP 30 mg Rx only packaged as a) 100 count unit dose… - a moderate-severity action.
NIFEdipine EXTENDED-RELEASE TABLETS, USP 30 mg Rx only packaged as a) 100 count unit dose… was recalled by The Harvard Drug Group in July 21, 2021. Reason: Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.. Check the official notice for the remedy. Verify recall #D-0652-2021 with the FDA Drug before acting.
The recall
The Harvard Drug Group issued this moderate-severity FDA Drug recall-Failed Dissolution Specification: Out of specification for dissolution during routine stability testing..
- Moderate
- severity level
- Class II
- classification
- July 21, 2021
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0652-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0652-2021) was formally reported on July 21, 2021, with the manufacturer initiating the action on July 2, 2021. It is classified under Moderate severity (Class II), with a current status of Terminated. The Harvard Drug Group is listed as the recalling firm, operating out of Livonia, MI. Federal records list the affected scope as 504 Cartons of 50 count each; 372 Cartons of 100 count each.
The documented reason for this recall is: Failed Dissolution Specification: Out of specification for dissolution during routine stability testing. Distribution data in the federal record shows the product reached: Distributed in OH and NJ. 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
504 Cartons of 50 count each; 372 Cartons of 100 count each
Related Recalls
6
5 from same agency
Product description
NIFEdipine EXTENDED-RELEASE TABLETS, USP 30 mg Rx only packaged as a) 100 count unit dose carton, NDC 0904-7080-61; b) 50 count unit dose carton, NDC 0904-7080-06: Distributed by: Ingenus Pharmaceuticals, LLC Orlando, FL 32839-6408 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA
Reason for recall
Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0652-2021 |
| Date reported | July 21, 2021 |
| Date initiated | July 2, 2021 |
| Recalling firm | The Harvard Drug Group |
| Firm location | Livonia, MI |
| Affected scope | 504 Cartons of 50 count each; 372 Cartons of 100 count each |
| Distribution | Distributed in OH and NJ |
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-0652-2021) 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? ▼
NIFEdipine EXTENDED-RELEASE TABLETS, USP 30 mg Rx only packaged as a) 100 count unit dose carton, NDC 0904-7080-61; b) 50 count unit dose carton, NDC 0904-7080-06: Distributed by: Ingenus Pharmaceuticals, LLC Orlando, FL 32839-6408 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA. Recalled by The Harvard Drug Group. Units affected: 504 Cartons of 50 count each; 372 Cartons of 100 count each.
Why was this product recalled? ▼
Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 21, 2021. Severity: Moderate. Recall number: D-0652-2021.
Where was the recalled product distributed? ▼
Distribution: Distributed in OH and NJ.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0652-2021) 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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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 July 21, 2021. 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.