Trizivir (abacavir recalls
The FDA has published 1 recall involving Trizivir (abacavir since 2012. The latest was reported on 18 Jul 2012. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls1since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 18 Jul 2012
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 100%Class III 0 0%
Why trizivir (abacavir is recalled
Companies
By year
All trizivir (abacavir recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Trizivir (abacavir sulfate 300mg, lamivudine 150 mg recalled | GlaxoSmithKline | Other | Nationwide |
Should you stop taking Trizivir (abacavir?
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.