Severity
Moderate
ModerateClass IICompleted
FDA Drug recall · Reported March 26, 2025
Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Slate Run Pharmaceuticals recalled Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Ph… - a moderate-severity action.
Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Ph… was recalled by Slate Run Pharmaceuticals in March 26, 2025. Reason: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.. Check the official notice for the remedy. Verify recall #D-0278-2025 with the FDA Drug before acting.
The recall
Slate Run Pharmaceuticals issued this moderate-severity FDA Drug recall-CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits..
- Moderate
- severity level
- Class II
- classification
- March 26, 2025
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0278-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0278-2025) was formally reported on March 26, 2025, with the manufacturer initiating the action on March 7, 2025. It is classified under Moderate severity (Class II), with a current status of Completed. Slate Run Pharmaceuticals is listed as the recalling firm, operating out of Columbus, OH. Federal records list the affected scope as 56,790 bottles.
The documented reason for this recall is: CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits. Distribution data in the federal record shows the product reached: Product was distributed to 8 distributors who may have further distribute the product 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 - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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
56,790 bottles
Related Recalls
6
0 from same agency
Product description
Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04
Reason for recall
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | D-0278-2025 |
| Date reported | March 26, 2025 |
| Date initiated | March 7, 2025 |
| Recalling firm | Slate Run Pharmaceuticals |
| Firm location | Columbus, OH |
| Affected scope | 56,790 bottles |
| Distribution | Product was distributed to 8 distributors who may have further distribute the product 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-0278-2025) 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? ▼
Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04. Recalled by Slate Run Pharmaceuticals. Units affected: 56,790 bottles.
Why was this product recalled? ▼
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 26, 2025. Severity: Moderate. Recall number: D-0278-2025.
Where was the recalled product distributed? ▼
Distribution: Product was distributed to 8 distributors who may have further distribute the product nationwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0278-2025) 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.
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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 March 26, 2025. 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.