Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported January 10, 2024
Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: Azurity Pharmaceuticals, Woburn, MA 01801, NDC 52652-9001-1
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Azurity Pharmaceuticals, Inc. recalled Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: … - a low-severity action.
Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: … was recalled by Azurity Pharmaceuticals, Inc. in January 10, 2024. Reason: Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topirama…. Check the official notice for the remedy. Verify recall #D-0213-2024 with the FDA Drug before acting.
The recall
Azurity Pharmaceuticals, Inc. issued this low-severity FDA Drug recall-Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topirama….
- Low
- severity level
- Class III
- classification
- January 10, 2024
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0213-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0213-2024) was formally reported on January 10, 2024, with the manufacturer initiating the action on December 8, 2023. It is classified under Low severity (Class III), with a current status of Terminated. Azurity Pharmaceuticals, Inc. is listed as the recalling firm, operating out of Wilmington, MA. Federal records list the affected scope as 2,220 bottles.
The documented reason for this recall is: Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months. 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 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
2,220 bottles
Related Recalls
6
5 from same agency
Product description
Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: Azurity Pharmaceuticals, Woburn, MA 01801, NDC 52652-9001-1
Reason for recall
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0213-2024 |
| Date reported | January 10, 2024 |
| Date initiated | December 8, 2023 |
| Recalling firm | Azurity Pharmaceuticals, Inc. |
| Firm location | Wilmington, MA |
| Affected scope | 2,220 bottles |
| 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-0213-2024) 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? ▼
Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: Azurity Pharmaceuticals, Woburn, MA 01801, NDC 52652-9001-1. Recalled by Azurity Pharmaceuticals, Inc.. Units affected: 2,220 bottles.
Why was this product recalled? ▼
Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 10, 2024. Severity: Low. Recall number: D-0213-2024.
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-0213-2024) 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 January 10, 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.