American Health Packaging recalls Anastrozole Tablets, USP, 1mg, 30-count unit dose blisters per carton, Rx Only, Packaged and Distributed by: American
American Health Packaging recalls 1mg Anastrozole tablets (NDC 60687-112-21) due to potential cross contamination from cleaning procedure failures. Affected lots expired by 08/31/2019 and 03/31/2020.
Lower-risk recall
GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Contact the company & request your remedy
What happened, in plain English
American Health Packaging is recalling 1mg Anastrozole tablets that may have been contaminated during manufacturing. This recall is due to potential cross contamination from cleaning procedure failures, which could affect patients taking the medication. Read more at govinfonow.com/recall/38826-american-health-packaging-recalls-anastrozole-tablets-due-to-potential-cross.
Source Summary by GovInfoNow · govinfonow.com/recall/38826-american-health-packaging-recalls-anastrozole-tablets-due-to-potential-cross · Updated October 5, 2026 · FDA enforcement record: FDA #D-1394-2019
Cite this page
“American Health Packaging Recalls Anastrozole Tablets Due to Potential Cross Contamination.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38826-american-health-packaging-recalls-anastrozole-tablets-due-to-potential-cross. Based on FDA recall #D-1394-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1394-2019%22&limit=1).
Why it’s dangerous
The recall is for potential cross contamination during manufacturing due to cleaning procedure failures. This could lead to unintended medication mix-ups, but the risk is not described as causing serious injury or death.
Who’s affected
Patients prescribed Anastrozole tablets by a healthcare provider. Those with specific lot numbers and expiration dates listed in the recall notice are most at risk.
How to tell if you have this one
Check for the product name 'Anastrozole Tablets, USP, 1mg, 30-count unit dose blisters per carton' with the NDC code 60687-112-21. Look for specific lot numbers: 175289A, 175286B, 175290B, 179906A, 183252A, or 184611A.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Product Details
Review the product label for the NDC code 60687-112-21 and specific lot numbers listed in the recall notice.
Questions people ask
Why is this product being recalled?
The recall is due to potential cross contamination from cleaning procedure failures during manufacturing.
What lot numbers are affected?
Affected lot numbers include 175289A, 175286B, 175290B, 179906A, 183252A, and 184611A.
Do I need to stop using this product?
No specific stop-use instruction is provided; the recall is for potential cross contamination, but the remedy is not stated.
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-1394-2019 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-1394-2019 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-1394-2019 (May 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1394-2019 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.