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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

Clindamycin Hydrochloride Capsules Recalled for Manufacturing Deviations

Agency Publication Date: April 28, 2025
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Summary

Preferred Pharmaceuticals, Inc. is recalling 1,190 bottles of Clindamycin Hydrochloride Capsules, USP (300mg), which were manufactured by Glenmark Pharmaceuticals Limited. The recall was initiated due to deviations from current Good Manufacturing Practice (cGMP) requirements. The affected product is packaged in 30-count bottles and includes nine specific lot numbers with an expiration date of July 31, 2026.

Risk

Deviations from manufacturing standards can compromise the quality and consistency of the medication. This may lead to the drug being less effective than intended or possessing unexpected quality issues, though no specific injuries have been reported.

What You Should Do

  1. This recall affects 30-count bottles of Clindamycin Hydrochloride Capsules, USP (300mg) distributed by Preferred Pharmaceuticals, Inc. under NDC 68788-8685-03.
  2. Check your prescription bottle for the following lot numbers: L0224T, K1824M, K0124N, J1624V, J0824O, I2424E, I1024O, A0925F, or L2324L. All affected lots have an expiration date of 7/31/2026.
  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 Preferred Pharmaceuticals, Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional information regarding this recall.

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: Clindamycin Hydrochloride Capsules, USP (300mg)
Variants: 300mg, 30-count bottle
Lot Numbers:
L0224T (Exp 7/31/2026)
K1824M (Exp 7/31/2026)
K0124N (Exp 7/31/2026)
J1624V (Exp 7/31/2026)
J0824O (Exp 7/31/2026)
I2424E (Exp 7/31/2026)
I1024O (Exp 7/31/2026)
A0925F (Exp 7/31/2026)
L2324L (Exp 7/31/2026)
NDC:
68788-8685-03

Manufactured by Glenmark Pharmaceuticals Limited; repackaged/distributed by Preferred Pharmaceuticals, Inc.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96756
Status: Active
Manufacturer: Preferred Pharmaceuticals, Inc.
Sold By: Pharmacies
Manufactured In: United States
Units Affected: 1190 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.