American Health Packaging Nabumetone Tablets Recall: Missing Medication Guide Label
American Health Packaging recalls 500mg Nabumetone Tablets due to missing Medication Guide label on carton. This affects prescription-only products sold from 2020 to 2021. Consumers should check labels for NDC 60687-374-01.
Lower-risk recall
Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with the accompanying Medication Guide was not included on the carton label.
Contact the company
What happened, in plain English
American Health Packaging is recalling prescription Nabumetone 500mg tablets because the carton label does not include the required Medication Guide. This means patients might not receive important safety information about the medication. Read more at govinfonow.com/recall/37056-american-health-packaging-nabumetone-tablets-recall-missing-medication-guide-label.
Source Summary by GovInfoNow · govinfonow.com/recall/37056-american-health-packaging-nabumetone-tablets-recall-missing-medication-guide-label · Updated October 5, 2026 · FDA enforcement record: FDA #D-1372-2020
Cite this page
“American Health Packaging Nabumetone Tablets Recall: Missing Medication Guide Label.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37056-american-health-packaging-nabumetone-tablets-recall-missing-medication-guide-label. Based on FDA recall #D-1372-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1372-2020%22&limit=1).
Why it’s dangerous
The medication guide is critical for understanding safe use of this NSAID painkiller. Without it, patients may miss important safety information about side effects and interactions.
Who’s affected
Prescription patients who received this specific Nabumetone tablet product from American Health Packaging. Those with the NDC carton number 60687-374-01 are most at risk.
How to tell if you have this one
Check for the NDC carton number 60687-374-01 on the packaging. The product was sold from 2020 to 2021 and is prescription-only.
- Brand
American Health Packaging- Category
Drug
What to do — step by step
Check Label
Look for the NDC carton number 60687-374-01 on the packaging to confirm if you have the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.1 years after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-1372-2020 (June 10, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1372-2020 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.