Lucid Pharma recalls
Lucid Pharma has 1 recall on record with the FDA and USDA, the earliest in 2017 and the latest reported on 28 Jun 2017. The most frequent reason is packaging defects.
Total recalls1since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 28 Jun 2017
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 lucid pharma is recalled
Product types
By year
All lucid pharma recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg recalled | Lucid Pharma | Packaging Defects | 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.