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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

Mckesson Packaging Services: Megestrol Acetate Oral Suspension Recalled for Subpotency

Agency Publication Date: February 8, 2018
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Summary

McKesson Packaging Services is recalling 24,120 cups of Megestrol Acetate Oral Suspension, USP 400 mg/10mL, which is a prescription medication used to treat loss of appetite and weight loss. This recall was initiated because the drug was found to be subpotent, meaning it did not meet the required strength specifications during stability testing. The affected medication was distributed in boxes containing 20 individual 10 mL unit-dose cups across the United States.

Risk

A subpotent drug may not provide the full intended dose of the medication, which can lead to reduced effectiveness of the treatment for the patient's condition.

What You Should Do

  1. Check your medication packaging for Megestrol Acetate Oral Suspension, USP 400 mg/10mL (10 mL unit-dose cups).
  2. Locate the lot number and expiration date on the individual cups or the box of 20 cups; this recall specifically affects Lot 0114588 with an expiration date of 10/18.
  3. If you identify affected medication, contact your healthcare provider or pharmacist immediately to discuss alternative treatment options and to ensure you are receiving the correct dosage.
  4. Return any unused portions of the recalled medication to the pharmacy where you purchased it for a refund and further instructions.
  5. Contact McKesson Packaging Services or the distributor at 7101 Weddington Rd Nw, Concord, NC 28027 for more information regarding this recall.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund
How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups)
Model:
NDC 63739-549-51
Recall #: D-0338-2018
Lot Numbers:
0114588 (Exp 10/18)
Date Ranges: October 2018

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79060
Status: Resolved
Manufacturer: Mckesson Packaging Services
Sold By: McKesson Packaging Services
Manufactured In: United States
Units Affected: 24120 cups
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.