Ben Venue Laboratories recalls
Ben Venue Laboratories has 6 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 27 Aug 2014. The most frequent reason is particulate matter.
Total recalls6since 2012
Last 12 months0reported
Class I233% of total
Ongoing0latest 27 Aug 2014
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 33%Class II 4 67%Class III 0 0%
Why ben venue laboratories is recalled
Product types
By year
All ben venue laboratories recalls, newest first
6 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | CYTARAbine for Injection USP, lyophiled in glass vials per vial recalled | Ben Venue Laboratories | Foreign Material | Nationwide |
| Drug | CLASS I | Acetylcysteine Solution, USP, 10% vial recalled | Ben Venue Laboratories | Particulate Matter | Nationwide |
| Drug | CLASS II | Leucovorin Calcium Injection USP, single use vials, 10mg/mL recalled | Ben Venue Laboratories | Particulate Matter | Nationwide |
| Drug | CLASS I | Vecuronium Bromide for Injection, For IV use only recalled | Ben Venue Laboratories | Particulate Matter | Nationwide |
| Drug | CLASS II | Midazolam HCl Injection, 5 mg/mL single use vials recalled | Ben Venue Laboratories | Packaging Defects | Nationwide |
| Drug | CLASS II | Octreotide Acetate Injection, 50 mcg/mL 05 mg/mL) single dose vials recalled | Ben Venue Laboratories | 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.