Purdue Pharma recalls
Purdue Pharma has 3 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 15 Nov 2017. The most frequent reason is potency & assay.
Total recalls3since 2015
Last 12 months0reported
Class I00% of total
Ongoing0latest 15 Nov 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 33%Class III 2 67%
Why purdue pharma is recalled
Product types
By year
All purdue pharma recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Betadine Solution Swabstick Povidone-Iodine Solution recalledBetadine | Purdue Pharma | Potency & Assay | Nationwide |
| Drug | CLASS III | Intermezzo (zolpidem tartrate) sublingual tablet 75 mg, CIV recalled | Purdue Pharma | Potency & Assay | 8 states |
| Drug | CLASS III | Intermezzo (zolpidem tartrate), sublingual tablet 5 mg recalled | Purdue Pharma | Potency & Assay | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.