Nabumetone recalls
The FDA has published 3 recalls involving Nabumetone since 2014. The latest was reported on 1 Jul 2020. Most were for labeling errors. American Health Packaging has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls3since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 1 Jul 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 33%Class III 2 67%
Why nabumetone is recalled
Companies
By year
All nabumetone recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Nabumetone Tablets, USP, 500 mg per carton x 10 blister cards) recalled | American Health Packaging | Packaging Defects | Nationwide |
| Drug | CLASS III | Nabumetone Tablets USP, 750 mg,Teva Pharmaceutical recalled | Teva Pharmaceuticals USA | Other | Nationwide |
| Drug | CLASS II | Nabumetone, Tablet, 500 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
Should you stop taking Nabumetone?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.