Biomet France SARL
Biomet France SARL appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0788-2016, Class II) was initiated on January 21, 2016.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 0
Known Names
biomet france sarl, biomet france s.a.r.l
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0788-2016 | Class II | Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or s | January 21, 2016 |