Zynrelef recalls
Zynrelef products have been recalled 1 time, most recently on 24 Aug 2022. The recalling company is usually Heron Therapeutics. The most common reason is packaging defects.
Total recalls1since 2022
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 Aug 2022
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 0 0%Class III 1 100%
Why zynrelef is recalled
Companies
Product types
By year
All zynrelef recalls, newest first
1 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Zynrelef (bupivacaine and meloxicam), 400 mg bupivacaine recalledZynrelef | Heron Therapeutics | 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.