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Drug recall · FDA · Published January 29, 2018

Mckesson Packaging Services recalls Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson

Mckesson Packaging Services recalls Megestrol Acetate Oral Suspension (400 mg/10mL) due to subpotent drug levels. This prescription medication may not contain enough active ingredient. Contact for details.

🇺🇸 FDA recall #D-0338-2018DrugMckesson Packaging Services ›
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Contact the company & request your remedy

Recalling firmMckesson Packaging Services7101 Weddington Rd Nw, N/A · Concord, NC 28027-3412
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Mckesson Packaging Services is recalling Megestrol Acetate Oral Suspension (400 mg/10mL) because it may not contain enough active ingredient. This prescription-only medication could be less effective than it should be, potentially affecting treatment outcomes. Read more at govinfonow.com/recall/40901-megestrol-acetate-oral-suspension-recall-subpotent-drug-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/40901-megestrol-acetate-oral-suspension-recall-subpotent-drug-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0338-2018

Cite this page

“Megestrol Acetate Oral Suspension Recall: Subpotent Drug Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40901-megestrol-acetate-oral-suspension-recall-subpotent-drug-risk. Based on FDA recall #D-0338-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0338-2018%22&limit=1).

Why it’s dangerous

The medication may have lower-than-stated active ingredient levels due to instability during testing. This could result in the product being less effective than intended for hormone therapy treatments.

Who’s affected

Prescription patients using Megestrol Acetate Oral Suspension (400 mg/10mL) from McKesson Packaging Services. Those with medical conditions requiring this hormone therapy are most at risk of treatment inefficiency.

How to tell if you have this one

Check for the product name 'Megestrol Acetate Oral Suspension, USP 400 mg/10mL' in boxes of 20 cups. Look for the lot number 0114588 with expiration date 10/18 on the packaging.

  • Brand
    Mckesson Packaging Services
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the lot number 0114588 and expiration date 10/18 on the packaging.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product may be less effective than intended due to subpotent drug levels, but it is not unsafe to use. Patients should consult their healthcare provider for guidance.

How can I get a replacement?

The recall record does not specify a replacement process or remedy.

What should I do if I have this product?

The recall record does not specify a remedy, so contact your healthcare provider for advice on whether to continue using the product.

Take action

Contact Mckesson Packaging Services

We’ve drafted a message you can send Mckesson Packaging Services to request your refund or repair — edit it as you like.

Subject: Recall D-0338-2018 — Mckesson Packaging Services Mckesson Packaging Services

Hello,

I own a Mckesson Packaging Services that is covered by recall D-0338-2018 from Mckesson Packaging Services.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0338-2018 (January 29, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0338-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA