Astora
Astora appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0279-2016, Class II) was initiated on October 26, 2015.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0279-2016 | Class II | MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. | October 26, 2015 |