Hydrocodone bitartrate and acetaminophen recalls
The FDA has published 11 recalls involving Hydrocodone bitartrate and acetaminophen since 2012. The latest was reported on 25 Nov 2020. Most were for potency & assay. 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 recalls11since 2012
Last 12 months0reported
Class I436% of total
Ongoing1latest 25 Nov 2020
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 4 36%Class II 4 36%Class III 3 27%
Why hydrocodone bitartrate and acetaminophen is recalled
Companies
By year
Ongoing hydrocodone bitartrate and acetaminophen recalls
1 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Hydrocodone Bitartrate and Acetaminophen Tablets, USP, 10 mg/500 mg recalled | Vintage Pharmaceuticals | Potency & Assay | Nationwide |
All hydrocodone bitartrate and acetaminophen recalls, newest first
11 totalShould you stop taking Hydrocodone bitartrate 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.