Meloxicam recalls
The FDA has published 4 recalls involving Meloxicam since 2012. The latest was reported on 3 Jan 2024. Most were for manufacturing (cgmp) deviations. Apotex 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 recalls4since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 3 Jan 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 100%Class III 0 0%
Why meloxicam is recalled
Companies
By year
All meloxicam recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Meloxicam Tablets, USP, 15 mg recalled by Cardinal HealthcareMeloxicam | Cardinal Healthcare | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Meloxicam Tablets, USP 5 mg recalled by Cardinal HealthMeloxicam | Cardinal Health | Manufacturing (CGMP) Deviations | FL, GA, SC |
| Drug | CLASS II | Meloxicam capsules, 12 mg recalled by South Coast Specialty | South Coast Specialty Compounding | Sterility | Nationwide |
| Drug | CLASS II | Meloxicam Tablets, USP, 15 mg recalled by Apotex | Apotex | Other | Nationwide |
Should you stop taking Meloxicam?
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.