American Health Packaging recalls Raloxifene Hydrochloride Tablets, USP, 60 mg, 30 Tablets (3 x 10 blister cards), Rx Only, Packaged and Distributed by:
American Health Packaging recalls 60mg Raloxifene Hydrochloride tablets due to failed dissolution testing. This may affect drug effectiveness. Contact for details.
Lower-risk recall
Failed Dissolution Specifications: Low out of specification results obtained during stability testing.
Contact the company & request your remedy
What happened, in plain English
American Health Packaging is recalling 60mg Raloxifene Hydrochloride tablets that failed stability testing. This could mean the medication doesn't work as intended, but the recall doesn't specify immediate danger to users. Read more at govinfonow.com/recall/37664-american-health-packaging-raloxifene-tablets-recall-failed-dissolution-testing.
Source Summary by GovInfoNow · govinfonow.com/recall/37664-american-health-packaging-raloxifene-tablets-recall-failed-dissolution-testing · Updated October 5, 2026 · FDA enforcement record: FDA #D-0854-2020
Cite this page
“American Health Packaging Raloxifene Tablets Recall: Failed Dissolution Testing.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37664-american-health-packaging-raloxifene-tablets-recall-failed-dissolution-testing. Based on FDA recall #D-0854-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0854-2020%22&limit=1).
Why it’s dangerous
The tablets failed dissolution testing during stability checks, meaning they may not release the active ingredient properly. This could affect how well the medication works over time, but the recall doesn't indicate immediate harm.
Who’s affected
Prescription users of Raloxifene Hydrochloride tablets who received this specific batch. People with medical conditions requiring this medication are most at risk.
How to tell if you have this one
Check for the NDC carton number 60687-266-21 or unit dose 60687-266-11. The lot number 180276A with expiration date 02/29/2020 is also part of this batch.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Product Details
Look for NDC carton 60687-266-21 or unit dose 60687-266-11 with lot number 180276A.
Questions people ask
Why is this product being recalled?
The tablets failed dissolution testing during stability checks, which may affect medication effectiveness.
Is there a risk of serious injury?
The recall does not mention any safety risks to users; it focuses on potential medication effectiveness issues.
How do I know if I have the recalled product?
Check for NDC carton 60687-266-21 or unit dose 60687-266-11 with lot number 180276A.
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-0854-2020 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-0854-2020 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-0854-2020 (December 4, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0854-2020 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.