Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

BluePoint Potassium Chloride Capsules Recalled for Dissolution Failure

Agency Publication Date: July 28, 2024
Share:
Sign in to monitor this recall

Summary

Amerisource Health Services LLC is recalling 61,231 bottles of Potassium Chloride Extended-Release Capsules, USP (750 mg, 10 mEq K) sold under the BluePoint Laboratories brand. The medication was found to fail dissolution specifications, meaning the capsules may not break down and release the active ingredient as intended. The recall affects several lots of 100-count and 500-count bottles with expiration dates ranging from July 2024 to September 2025.

Risk

If the medication fails to dissolve properly, patients may receive an incorrect dose of potassium, potentially leading to poorly managed potassium levels. This can cause serious health complications if blood potassium levels are not maintained within the target range.

What You Should Do

  1. The recalled products are BluePoint Laboratories Potassium Chloride Extended-Release Capsules (750 mg, 10 mEq K) packaged in 100-count and 500-count bottles.
  2. Identify the affected products by checking the label for NDC 68001-396-00 (100-count bottles) or NDC 68001-396-03 (500-count bottles). See the Affected Products section below for the full list of affected codes.
  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 the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

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: Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K, 100-count bottleby BluePoint Laboratories
Variants: 100-count bottle, 750 mg, 10 mEq K
Lot Numbers:
17221738 (Exp 07/31/2024)
17222494 (Exp 10/31/2024)
17230533 (Exp 01/31/2025)
17232208 (Exp 09/30/2025)
NDC:
68001-396-00

Manufactured by Glenmark Pharmaceuticals Ltd.; Distributed for BluePoint Laboratories.

Product: Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K, 500-count bottleby BluePoint Laboratories
Variants: 500-count bottle, 750 mg, 10 mEq K
Lot Numbers:
17221823 (Exp 07/31/2024)
17221830 (Exp 07/31/2024)
17221831 (Exp 08/31/2024)
17230248 (Exp 12/31/2024)
17230253 (Exp 12/31/2024)
17230271 (Exp 12/31/2024)
17230796 (Exp 02/28/2025)
17230820 (Exp 02/28/2025)
17230825 (Exp 03/31/2025)
17230833 (Exp 03/31/2025)
17230840 (Exp 03/31/2025)
17231537 (Exp 06/30/2025)
17231540 (Exp 06/30/2025)
17231719 (Exp 06/30/2025)
17231737 (Exp 06/30/2025)
17232111 (Exp 09/30/2025)
17232164 (Exp 09/30/2025)
NDC:
68001-396-03

Manufactured by Glenmark Pharmaceuticals Ltd.; Distributed for BluePoint Laboratories.

Product Images

Label, Glenmark Potassium Chloride Extended Release 750mg Capsules, 100 count

Label, Glenmark Potassium Chloride Extended Release 750mg Capsules, 100 count

Label, Glenmark Potassium Chloride Extended Release 750mg Capsules, 500 count

Label, Glenmark Potassium Chloride Extended Release 750mg Capsules, 500 count

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94946
Status: Active
Manufacturer: Amerisource Health Services LLC
Sold By: Pharmacies; Healthcare Distributors
Manufactured In: India, United States
Units Affected: 61,231 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 FDA Press Release 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.