Marbeta L Kit recalls
Marbeta L Kit products have been recalled 1 time, most recently on 17 Apr 2019. The recalling company is usually Aurobindo Pharma USA. The most common reason is particulate matter.
Total recalls1since 2019
Last 12 months0reported
Class I1100% of total
Ongoing0latest 17 Apr 2019
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 100%Class II 0 0%Class III 0 0%
Why marbeta l kit is recalled
Companies
Product types
By year
All marbeta l kit recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Lidocaine HCl Injection, USP 1 % 50 mg/ (10 mg/mL) vial recalledMarbeta L Kit | Aurobindo Pharma USA | Particulate Matter | NC, NM |
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.