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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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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

BluePoint Metoprolol Succinate Extended-Release Tablets Recalled

Agency Publication Date: February 15, 2023
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Summary

Amerisource Health Services LLC is recalling 6,670 100-count bottles and 2,666 500-count bottles of BluePoint Laboratories Metoprolol Succinate Extended-Release Tablets (50 mg), a medication used to treat high blood pressure and chest pain. This recall was initiated because the tablets failed dissolution tests, meaning the medication may not be released into the body at the correct rate. No incidents or injuries have been reported to date regarding this issue.

Risk

Failed dissolution means the medication may not be absorbed by the body as intended, which could lead to ineffective treatment of blood pressure or heart conditions. This poses a moderate risk to patients who rely on consistent dosing to manage cardiovascular health.

What You Should Do

  1. This recall affects Metoprolol Succinate Extended-Release Tablets (50 mg) sold in 100-count bottles (NDC 68001-501-00) and 500-count bottles (NDC 68001-501-03) under the BluePoint Laboratories brand.
  2. Check your medication bottles for the following lot numbers and expiration dates: lot 21143211 (expires 03/31/2023) for 100-count bottles; and lots 21143185 or 21143193 (both expire 02/28/2023) for 500-count bottles.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Amerisource Health Services LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional information regarding consumer safety.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Metoprolol Succinate Extended-Release Tablets (50 mg)by BluePoint Laboratories
Variants: 50 mg, Extended-Release Tablets, 100-count bottle, 500-count bottle
Lot Numbers:
21143211 (Exp 03/31/2023)
21143185 (Exp 02/28/2023)
21143193 (Exp 02/28/2023)
NDC:
68001-501-00
68001-501-03

Manufactured by Alkem Laboratories Ltd., India.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91528
Status: Resolved
Manufacturer: Amerisource Health Services LLC
Sold By: BluePoint Laboratories; Amerisource Health Services LLC
Manufactured In: India, United States
Units Affected: (a) 6670 100-count (b) 2666 500-count bottles
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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.