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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

Succinylcholine Chloride Injection Recalled for Low Preservative Levels

Agency Publication Date: October 7, 2025
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Summary

Dr. Reddy's Laboratories, Inc. is recalling 571 vials of Succinylcholine Chloride Injection, USP (200 mg/10 mL). Stability testing at the six-month mark revealed that the concentration of the preservative in the medication had decreased below required specifications. This recall affects multiple-dose vials distributed nationwide across the United States.

Risk

A decreased concentration of preservative in a multiple-dose vial may fail to prevent the growth of microorganisms once the vial is opened, potentially leading to infections in patients who receive the injection.

What You Should Do

  1. Stop using the recalled product immediately.
  2. Check your inventory for Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL) in 25 x 10 mL Multiple-Dose Vials with NDC 43598-666-25 and Lot # K250048.
  3. Contact Dr. Reddy's Laboratories, Inc. or your distributor to arrange for the return of any affected vials.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions or wish to report a problem.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Succinylcholine Chloride Injection, USP (200 mg/10 mL)
Variants: 20 mg/mL, 25 x 10 mL Multiple-Dose Vials, Intravenous or Intramuscular use
Lot Numbers:
K250048
NDC:
43598-666-25

Recall #: D-0008-2026; Rx Only.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97690
Status: Active
Manufacturer: Dr. Reddy's Laboratories, Inc.
Sold By: Wholesalers; Hospitals; Surgical Centers
Manufactured In: United States
Units Affected: 571 vials
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.