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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

Arbor Pharmaceuticals Inc.: Nymalize (nimodipine) Oral Solution Recalled Due to Subpotency

Agency Publication Date: September 28, 2020
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Summary

Arbor Pharmaceuticals Inc. is recalling 1,846 cartons of Nymalize (nimodipine) oral solution, 60 mg/20 mL, because the medication was found to be subpotent. This prescription drug, used to treat certain types of brain bleeding, contains less of the active ingredient than required. Affected products were distributed nationwide in the United States and include 12 unit-dose cups and 12 oral syringes per carton.

Risk

A subpotent drug may not provide the full intended dose, potentially leading to a lack of effectiveness in managing the patient's condition. While the risk level is classified as low, failing to receive the proper dosage of nimodipine could impact the treatment of serious medical conditions.

What You Should Do

  1. Identify your medication by checking the outer shipping carton and inner packaging for Nymalize (nimodipine) oral solution, 60 mg/20 mL (NDC 24338-200-12).
  2. Check the package for lot number 356884 with an expiration date of 11/30/2021 to see if your product is included in this recall.
  3. Contact your healthcare provider or pharmacist immediately for guidance if you have been using the affected medication.
  4. Return any unused product from the affected lot to your pharmacy for a refund.
  5. Contact Arbor Pharmaceuticals Inc. directly at their Atlanta, GA headquarters if you have further questions regarding the return process.
  6. For additional information or to report a problem, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Nymalize (nimodipine) oral solution, 60 mg/20 mL
Model:
NDC 24338-200-12
Recall #: D-1625-2020
Lot Numbers:
356884 (Exp. 11/30/2021)
Date Ranges: Expires 11/30/2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86392
Status: Resolved
Manufacturer: Arbor Pharmaceuticals Inc.
Sold By: pharmacies
Manufactured In: United States
Units Affected: 1846 cartons
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.