Procrit (epoetin Alfa recalls
The FDA has published 1 recall involving Procrit (epoetin Alfa since 2012. The latest was reported on 26 Dec 2012. Most were for particulate matter. 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 26 Dec 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 procrit (epoetin alfa is recalled
Companies
By year
All procrit (epoetin alfa recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Procrit (epoetin alfa) injection/mL vial recalled | Physicians Total Care | Particulate Matter | CA, PA |
Should you stop taking Procrit (epoetin Alfa?
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.