Oxycodone and acetaminophen recalls
The FDA has published 4 recalls involving Oxycodone and acetaminophen since 2013. The latest was reported on 5 Sep 2018. Most were for labeling errors. Watson Laboratories 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 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 5 Sep 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 50%Class III 2 50%
Why oxycodone and acetaminophen is recalled
Companies
By year
All oxycodone and acetaminophen recalls, newest first
4 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg recalled | Mayne Pharma | Labeling Errors | Nationwide |
| Drug | CLASS II | Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg recalled by Alvogen | Alvogen | Other | Nationwide |
| Drug | CLASS II | Oxycodone and Acetaminophen Tablets, USP 10 mg/650 mg, CII recalled | Watson Laboratories | Packaging Defects | Nationwide |
| Drug | CLASS III | Oxycodone and Acetaminophen Capsules, USP 5mg/500 mg recalled | Watson Laboratories | Potency & Assay | Nationwide |
Should you stop taking Oxycodone and acetaminophen?
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.