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Drug recall · FDA · Published May 9, 2019

American Health Packaging recalls Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only,

American Health Packaging recalls 30-count and 1000-count Anastrozole Tablets (NDC 68001-155-04 and 68001-155-08) manufactured with potential cross contamination risks. Rx only products affected by GMP deviations in cleaning procedures.

🇺🇸 FDA recall #D-1467-2019DrugAmerican Health Packaging ›
Take action

Contact the company & request your remedy

Recalling firmAmerican Health Packaging2550 John Glenn Ave Ste A · Columbus, OH 43217-1188
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

American Health Packaging has recalled certain Anastrozole Tablets (1 mg) due to potential cross contamination from cleaning procedure failures. This recall affects prescription-only products that may pose a risk of contamination to patients. Read more at govinfonow.com/recall/38825-american-health-packaging-recalls-anastrozole-tablets-due-to-potential-cross.

Source Summary by GovInfoNow · govinfonow.com/recall/38825-american-health-packaging-recalls-anastrozole-tablets-due-to-potential-cross · Updated October 5, 2026 · FDA enforcement record: FDA #D-1467-2019

Cite this page

“American Health Packaging Recalls Anastrozole Tablets Due to Potential Cross Contamination.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38825-american-health-packaging-recalls-anastrozole-tablets-due-to-potential-cross. Based on FDA recall #D-1467-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1467-2019%22&limit=1).

Why it’s dangerous

The recall is due to potential cross contamination from cleaning procedure failures during manufacturing. This could lead to unintended substances being present in the medication, though the exact risk level is not specified in the recall notice.

Who’s affected

Prescription patients using the recalled Anastrozole Tablets (1 mg) from specific lots and expiration dates. Those with medical conditions requiring hormone therapy are most at risk.

How to tell if you have this one

Check for 30-count or 1000-count Anastrozole Tablets (1 mg) with NDC numbers 68001-155-04 or 68001-155-08. Look for specific lot numbers and expiration dates listed in the recall notice.

  • Brand
    American Health Packaging
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Identify the product by checking the NDC numbers and lot numbers listed in the recall notice.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall states there is a potential for cross contamination due to cleaning procedure failures, but the exact risk level is not specified. Consult your healthcare provider for advice.

What should I do if I have the recalled product?

The recall does not specify a remedy, so contact American Health Packaging directly for guidance on next steps.

Are there any specific lot numbers I should check?

Yes, check the specific lot numbers and expiration dates listed in the recall notice for the 30-count and 1000-count bottles.

Take action

Contact American Health Packaging

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

Subject: Recall D-1467-2019 — American Health Packaging American Health Packaging

Hello,

I own a American Health Packaging that is covered by recall D-1467-2019 from American Health Packaging.

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-1467-2019 (May 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1467-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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