American Health Packaging recalls Doxycycline Hyclate Tablets, USP, 100 mg, 30 Tablets per carton (3 x 10 Unit Dose Blisters), Rx Only, Distributed by:
American Health Packaging recalls 100mg Doxycycline Hyclate Tablets due to failed dissolution test. These prescription-only tablets may not release medication properly. Consumers should contact the manufacturer for details.
Lower-risk recall
Failed Dissolution Specifications: Out of specification result for the dissolution test.
Contact the company & request your remedy
What happened, in plain English
American Health Packaging is recalling prescription doxycycline hyclate tablets that failed dissolution testing. This means the medication might not release properly in the body, potentially reducing effectiveness. Read more at govinfonow.com/recall/39834-american-health-packaging-doxycycline-tablets-recall-failed-dissolution-test.
Source Summary by GovInfoNow · govinfonow.com/recall/39834-american-health-packaging-doxycycline-tablets-recall-failed-dissolution-test · Updated October 6, 2026 · FDA enforcement record: FDA #D-1582-2019
Cite this page
“American Health Packaging Doxycycline Tablets Recall: Failed Dissolution Test.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39834-american-health-packaging-doxycycline-tablets-recall-failed-dissolution-test. Based on FDA recall #D-1582-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1582-2019%22&limit=1).
Why it’s dangerous
The tablets failed dissolution testing, meaning they may not release the medication properly in the body. This could lead to reduced effectiveness of the drug. However, the recall does not indicate a risk of serious injury or harm.
Who’s affected
Prescription holders of the 100mg doxycycline hyclate tablets with NDC 62584-693-21 (carton) or 62584-693-11 (unit dose) are affected. Patients who have taken these tablets should consult their doctor.
How to tell if you have this one
Check for the NDC carton number 62584-693-21 or unit dose number 62584-693-11 on the packaging. The tablets are prescription-only and were distributed by American Health Packaging.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Product Details
Look for NDC carton number 62584-693-21 or unit dose number 62584-693-11 on the packaging.
Questions people ask
Why is this product being recalled?
The tablets failed dissolution testing, meaning they may not release medication properly in the body.
What should I do if I have this product?
Contact American Health Packaging for details on the recall and next steps.
Is there a risk of serious injury from these tablets?
The recall does not indicate a risk of serious injury or harm.
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-1582-2019 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-1582-2019 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-1582-2019 (August 1, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1582-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.