Device recall
Z-2310-2010: Genzyme Biosurgery Essentials Kit, Item Number 82004
FDA device recall · Class II · Genzyme Corporation
Key facts
| Recall number (Z-number) | Z-2310-2010 |
|---|---|
| Recall event | 56218 |
| Product | Genzyme Biosurgery Essentials Kit, Item Number 82004 |
| Product code | LRO |
| Recalling firm | Genzyme Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 30, 2012 |
| FEI number | 3002836339 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database