American Health Packaging recalls Aspirin and Extended-release Dipyridamole Capsules, 25 mg/200 mg, 20 capsules per carton (5 blister cards x 4 unit
American Health Packaging recalls Aspirin and Extended-release Dipyridamole Capsules due to potential unknown impurities in stability samples. Affected lots expire by March 2019.
Recall notice
Failed Impurities/Degradation Specifications; out of specification result for an unknown impurity in stability samples.
Contact the company & request your remedy
What happened, in plain English
American Health Packaging is recalling Aspirin and Extended-release Dipyridamole Capsules because stability testing found an unknown impurity. This could pose a risk to users taking these medications. Read more at govinfonow.com/recall/39139-american-health-packaging-aspirin-recall-unknown-impurity-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39139-american-health-packaging-aspirin-recall-unknown-impurity-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1820-2019
Cite this page
“American Health Packaging Aspirin Recall: Unknown Impurity Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39139-american-health-packaging-aspirin-recall-unknown-impurity-risk. Based on FDA recall #D-1820-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1820-2019%22&limit=1).
Why it’s dangerous
The recall is based on stability testing showing an unknown impurity in the medication. This impurity could potentially affect the medication's safety and effectiveness, though the exact risk is not specified.
Who’s affected
People who have the recalled Aspirin or Extended-release Dipyridamole Capsules, typically prescribed by a doctor. Those with specific medical conditions requiring these medications are at higher risk.
How to tell if you have this one
Check for the NDC Carton number 60687-305-32 or Blister Pack number 60687-305-33. The affected lots include specific expiration dates from March 2019 through November 2019.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC Carton number 60687-305-32 or Blister Pack number 60687-305-33 on the packaging.
Questions people ask
Why is this medication being recalled?
The recall is due to stability testing finding an unknown impurity in the medication, which could affect safety and effectiveness.
What lots are affected?
Affected lots include 174262 (exp. 03/31/2019), 176469 (exp. 06/30/2019), 177897 (exp. 08/31/2019), 178318 and 178436 (exp. 09/30/2019), and 179547 and 179656 (exp. 11/30/2019).
Do I need to stop using these medications?
The recall does not specify a stop-use instruction, so users should check the product details to confirm if they have the affected lots.
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-1820-2019 — American Health Packaging American Health Packaging Hello, I own a American Health Packaging that is covered by recall D-1820-2019 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-1820-2019 (March 1, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1820-2019 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.